Canonical Allele Identifier: CA150690527

Gene:

Linked Data

• dbSNP Id: rs928973148
• gnomAD v2: 6-156133831-A-G
• gnomAD v3: 6-155812697-A-G
• gnomAD v4: 6-155812697-A-G
• MyVariant Identifiers: chr6:g.156133831A>G (hg19) ; chr6:g.155812697A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.155812697A>G , CM000668.2:g.155812697A>G	GRCh38
NC_000006.11:g.156133831A>G , CM000668.1:g.156133831A>G	GRCh37
NC_000006.10:g.156175523A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_943142.1:n.79+19278A>G
XR_943146.1:n.645-658T>C
XR_001744423.1:n.699-658T>C
XR_001744424.1:n.79+19278A>G