Canonical Allele Identifier: CA961070414

Gene: MYH7

Linked Data

• dbSNP Id: rs776778917
• gnomAD v3: 14-23431695-G-C
• gnomAD v4: 14-23431695-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23431695G>C , CM000676.2:g.23431695G>C	GRCh38
NC_000014.8:g.23900904G>C , CM000676.1:g.23900904G>C	GRCh37
NC_000014.7:g.22970744G>C	NCBI36
NG_007884.1:g.8967C>G , LRG_384:g.8967C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000355349.4:c.640-18C>G MANE Select	ENSP00000347507.3:n.640-18C>G
ENST00000355349.3:c.640-18C>G	ENSP00000347507.3:n.640-18C>G
NM_000257.3:c.640-18C>G	NP_000248.2:n.640-18C>G
XR_245686.3:n.746-18C>G
XM_017021340.1:c.640-18C>G	XP_016876829.1:n.640-18C>G
NM_000257.4:c.640-18C>G MANE Select	NP_000248.2:n.640-18C>G