Canonical Allele Identifier: CA571581060

Gene:

Linked Data

• dbSNP Id: rs769241177
• gnomAD v2: 6-156133459-C-A
• MyVariant Identifiers: chr6:g.156133459C>A (hg19) ; chr6:g.155812325C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.155812325C>A , CM000668.2:g.155812325C>A	GRCh38
NC_000006.11:g.156133459C>A , CM000668.1:g.156133459C>A	GRCh37
NC_000006.10:g.156175151C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943142.1:n.79+18906C>A
XR_943146.1:n.645-286G>T
XR_001744423.1:n.699-286G>T
XR_001744424.1:n.79+18906C>A