Canonical Allele Identifier: CA257819358
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs902687469
MyVariant Identifiers: chr14:g.23894028T>A (hg19) chr14:g.23424819T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23424819T>A , CM000676.2:g.23424819T>A GRCh38
NC_000014.8:g.23894028T>A , CM000676.1:g.23894028T>A GRCh37
NC_000014.7:g.22963868T>A NCBI36
NG_007884.1:g.15843A>T , LRG_384:g.15843A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.2629A>T MANE Select ENSP00000347507.3:p.Met877Leu
ENST00000355349.3:c.2629A>T ENSP00000347507.3:p.Met877Leu
NM_000257.3:c.2629A>T NP_000248.2:p.Met877Leu
XR_245686.3:n.2735A>T
XM_017021340.1:c.2629A>T XP_016876829.1:p.Met877Leu
NM_000257.4:c.2629A>T MANE Select NP_000248.2:p.Met877Leu
Search 100 bp 5'
Search 100 bp 3'