Canonical Allele Identifier: CA485766274

Linked Data

ClinVar Variation Id: 1083411
ClinVar RCV Id: RCV001400047
dbSNP Id: rs1892175008
MyVariant Identifiers: chr14:g.23884994C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415785C>T , CM000676.2:g.23415785C>T GRCh38
NC_000014.8:g.23884994C>T , CM000676.1:g.23884994C>T GRCh37
NC_000014.7:g.22954834C>T NCBI36
NG_007884.1:g.24877G>A , LRG_384:g.24877G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.5001G>A (MYH7) MANE Select ENSP00000347507.3:p.Leu1667=
ENST00000355349.3:c.5001G>A (MYH7) ENSP00000347507.3:p.Leu1667=
NM_000257.3:c.5001G>A (MYH7) NP_000248.2:p.Leu1667=
NR_126491.1:n.217C>T (MHRT)
XM_017021340.1:c.5001G>A (MYH7) XP_016876829.1:p.Leu1667=
NM_000257.4:c.5001G>A (MYH7) MANE Select NP_000248.2:p.Leu1667=