Canonical Allele Identifier: CA257825801

Gene: MYH7

Linked Data

• dbSNP Id: rs112361904
• MyVariant Identifiers: chr14:g.23900626C>T (hg19) ; chr14:g.23431417C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23431417C>T , CM000676.2:g.23431417C>T	GRCh38
NC_000014.8:g.23900626C>T , CM000676.1:g.23900626C>T	GRCh37
NC_000014.7:g.22970466C>T	NCBI36
NG_007884.1:g.9245G>A , LRG_384:g.9245G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000355349.4:c.796+1G>A MANE Select	ENSP00000347507.3:n.796+1G>A
ENST00000355349.3:c.796+1G>A	ENSP00000347507.3:n.796+1G>A
NM_000257.3:c.796+1G>A	NP_000248.2:n.796+1G>A
XR_245686.3:n.902+1G>A
XM_017021340.1:c.796+1G>A	XP_016876829.1:n.796+1G>A
NM_000257.4:c.796+1G>A MANE Select	NP_000248.2:n.796+1G>A