Canonical Allele Identifier: CA150690520

Gene:

Linked Data

• dbSNP Id: rs988754344
• gnomAD v3: 6-155812637-T-A
• gnomAD v4: 6-155812637-T-A
• MyVariant Identifiers: chr6:g.156133771T>A (hg19) ; chr6:g.155812637T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.155812637T>A , CM000668.2:g.155812637T>A	GRCh38
NC_000006.11:g.156133771T>A , CM000668.1:g.156133771T>A	GRCh37
NC_000006.10:g.156175463T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943142.1:n.79+19218T>A
XR_943146.1:n.645-598A>T
XR_001744423.1:n.699-598A>T
XR_001744424.1:n.79+19218T>A