Canonical Allele Identifier: CA150690512

Gene:

Linked Data

• dbSNP Id: rs148591275
• gnomAD v3: 6-155812598-C-T
• gnomAD v4: 6-155812598-C-T
• MyVariant Identifiers: chr6:g.156133732C>T (hg19) ; chr6:g.155812598C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.155812598C>T , CM000668.2:g.155812598C>T	GRCh38
NC_000006.11:g.156133732C>T , CM000668.1:g.156133732C>T	GRCh37
NC_000006.10:g.156175424C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943142.1:n.79+19179C>T
XR_943146.1:n.645-559G>A
XR_001744423.1:n.699-559G>A
XR_001744424.1:n.79+19179C>T