Canonical Allele Identifier: CA961071879

Gene: MYH7

Linked Data

• dbSNP Id: rs1892437917
• gnomAD v3: 14-23420639-TA-T
• gnomAD v4: 14-23420639-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23420644del , CM000676.2:g.23420644del	GRCh38
NC_000014.8:g.23889853del , CM000676.1:g.23889853del	GRCh37
NC_000014.7:g.22959693del	NCBI36
NG_007884.1:g.20022del , LRG_384:g.20022del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3336+318del MANE Select	ENSP00000347507.3:n.3336+318del
ENST00000355349.3:c.3336+318del	ENSP00000347507.3:n.3336+318del
NM_000257.3:c.3336+318del	NP_000248.2:n.3336+318del
XR_245686.3:n.3444+318del
XM_017021340.1:c.3336+318del	XP_016876829.1:n.3336+318del
NM_000257.4:c.3336+318del MANE Select	NP_000248.2:n.3336+318del