Canonical Allele Identifier: CA389037865
Gene: MYH7 HGNC NCBI
MHRT HGNC NCBI

Linked Data

dbSNP Id: rs1263708425
gnomAD v2: 14-23885482-G-C
gnomAD v4: 14-23416273-G-C
MyVariant Identifiers: chr14:g.23885482G>C (hg19) chr14:g.23416273G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23416273G>C , CM000676.2:g.23416273G>C GRCh38
NC_000014.8:g.23885482G>C , CM000676.1:g.23885482G>C GRCh37
NC_000014.7:g.22955322G>C NCBI36
NG_007884.1:g.24389C>G , LRG_384:g.24389C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4684C>G (MYH7) MANE Select ENSP00000347507.3:p.Gln1562Glu
ENST00000355349.3:c.4684C>G (MYH7) ENSP00000347507.3:p.Gln1562Glu
NM_000257.3:c.4684C>G (MYH7) NP_000248.2:p.Gln1562Glu
NR_126491.1:n.534G>C (MHRT)
XM_017021340.1:c.4684C>G (MYH7) XP_016876829.1:p.Gln1562Glu
NM_000257.4:c.4684C>G (MYH7) MANE Select NP_000248.2:p.Gln1562Glu
Search 100 bp 5'
Search 100 bp 3'