Canonical Allele Identifier: CA485622896

Gene: MYH7

Linked Data

• gnomAD v4: 14-23425404-G-T
• MyVariant Identifiers: chr14:g.23894613G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23425404G>T , CM000676.2:g.23425404G>T	GRCh38
NC_000014.8:g.23894613G>T , CM000676.1:g.23894613G>T	GRCh37
NC_000014.7:g.22964453G>T	NCBI36
NG_007884.1:g.15258C>A , LRG_384:g.15258C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.2301C>A MANE Select	ENSP00000347507.3:p.Ala767=
ENST00000355349.3:c.2301C>A	ENSP00000347507.3:p.Ala767=
NM_000257.3:c.2301C>A	NP_000248.2:p.Ala767=
XR_245686.3:n.2407C>A
XM_017021340.1:c.2301C>A	XP_016876829.1:p.Ala767=
NM_000257.4:c.2301C>A MANE Select	NP_000248.2:p.Ala767=