Canonical Allele Identifier: CA1063282027

Gene:

Linked Data

• dbSNP Id: rs1577990839
• gnomAD v3: 4-62557828-A-C
• gnomAD v4: 4-62557828-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.62557828A>C , CM000666.2:g.62557828A>C	GRCh38
NC_000004.11:g.63423546A>C , CM000666.1:g.63423546A>C	GRCh37
NC_000004.10:g.63106141A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_938814.1:n.161-6016A>C