Canonical Allele Identifier: CA150690513

Gene:

Linked Data

• dbSNP Id: rs111659464
• gnomAD v2: 6-156133734-A-G
• gnomAD v3: 6-155812600-A-G
• gnomAD v4: 6-155812600-A-G
• MyVariant Identifiers: chr6:g.156133734A>G (hg19) ; chr6:g.155812600A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.155812600A>G , CM000668.2:g.155812600A>G	GRCh38
NC_000006.11:g.156133734A>G , CM000668.1:g.156133734A>G	GRCh37
NC_000006.10:g.156175426A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943142.1:n.79+19181A>G
XR_943146.1:n.645-561T>C
XR_001744423.1:n.699-561T>C
XR_001744424.1:n.79+19181A>G