Canonical Allele Identifier: CA150690522

Gene:

Linked Data

• dbSNP Id: rs17086680
• gnomAD v2: 6-156133784-G-A
• gnomAD v3: 6-155812650-G-A
• gnomAD v4: 6-155812650-G-A
• MyVariant Identifiers: chr6:g.156133784G>A (hg19) ; chr6:g.155812650G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.155812650G>A , CM000668.2:g.155812650G>A	GRCh38
NC_000006.11:g.156133784G>A , CM000668.1:g.156133784G>A	GRCh37
NC_000006.10:g.156175476G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943142.1:n.79+19231G>A
XR_943146.1:n.645-611C>T
XR_001744423.1:n.699-611C>T
XR_001744424.1:n.79+19231G>A