Canonical Allele Identifier: CA150690488

Gene:

Linked Data

• dbSNP Id: rs913101722
• gnomAD v2: 6-156133556-C-T
• gnomAD v3: 6-155812422-C-T
• gnomAD v4: 6-155812422-C-T
• MyVariant Identifiers: chr6:g.156133556C>T (hg19) ; chr6:g.155812422C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.155812422C>T , CM000668.2:g.155812422C>T	GRCh38
NC_000006.11:g.156133556C>T , CM000668.1:g.156133556C>T	GRCh37
NC_000006.10:g.156175248C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943142.1:n.79+19003C>T
XR_943146.1:n.645-383G>A
XR_001744423.1:n.699-383G>A
XR_001744424.1:n.79+19003C>T