Canonical Allele Identifier: CA257825630

Gene: MYH7

Linked Data

• dbSNP Id: rs112639546
• MyVariant Identifiers: chr14:g.23900209C>A (hg19) ; chr14:g.23431000C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23431000C>A , CM000676.2:g.23431000C>A	GRCh38
NC_000014.8:g.23900209C>A , CM000676.1:g.23900209C>A	GRCh37
NC_000014.7:g.22970049C>A	NCBI36
NG_007884.1:g.9662G>T , LRG_384:g.9662G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.797-1G>T MANE Select	ENSP00000347507.3:n.797-1G>T
ENST00000355349.3:c.797-1G>T	ENSP00000347507.3:n.797-1G>T
NM_000257.3:c.797-1G>T	NP_000248.2:n.797-1G>T
XR_245686.3:n.903-1G>T
XM_017021340.1:c.797-1G>T	XP_016876829.1:n.797-1G>T
NM_000257.4:c.797-1G>T MANE Select	NP_000248.2:n.797-1G>T