Canonical Allele Identifier: CA150690509

Gene:

Linked Data

• dbSNP Id: rs1016774726
• gnomAD v3: 6-155812571-T-C
• gnomAD v4: 6-155812571-T-C
• MyVariant Identifiers: chr6:g.156133705T>C (hg19) ; chr6:g.155812571T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.155812571T>C , CM000668.2:g.155812571T>C	GRCh38
NC_000006.11:g.156133705T>C , CM000668.1:g.156133705T>C	GRCh37
NC_000006.10:g.156175397T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943142.1:n.79+19152T>C
XR_943146.1:n.645-532A>G
XR_001744423.1:n.699-532A>G
XR_001744424.1:n.79+19152T>C