Canonical Allele Identifier: CA350348921
Gene: BMPR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.203420964A>C (hg19) chr2:g.202556241A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202556241A>C , CM000664.2:g.202556241A>C GRCh38
NC_000002.11:g.203420964A>C , CM000664.1:g.203420964A>C GRCh37
NC_000002.10:g.203129209A>C NCBI36
NG_009363.1:g.184915A>C , LRG_712:g.184915A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.2576A>C MANE Select ENSP00000363708.4:p.Asn859Thr
ENST00000638587.1:c.2507A>C ENSP00000491062.1:n.2507A>C
ENST00000374574.2:c.1586+3353A>C ENSP00000363702.2:n.1586+3353A>C
ENST00000374580.8:c.2576A>C ENSP00000363708.4:p.Asn859Thr
NM_001204.6:c.2576A>C , LRG_712t1:c.2576A>C NP_001195.2:p.Asn859Thr
XM_011511687.1:c.2576A>C XP_011509989.1:p.Asn859Thr
XM_011511688.1:c.1586+3353A>C XP_011509990.1:n.1586+3353A>C
NM_001204.7:c.2576A>C MANE Select NP_001195.2:p.Asn859Thr
Search 100 bp 5'
Search 100 bp 3'