Canonical Allele Identifier: CA1096189924

Gene:

Linked Data

• dbSNP Id: rs1778929536
• gnomAD v3: 6-155817672-T-C
• gnomAD v4: 6-155817672-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.155817672T>C , CM000668.2:g.155817672T>C	GRCh38
NC_000006.11:g.156138806T>C , CM000668.1:g.156138806T>C	GRCh37
NC_000006.10:g.156180498T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943142.1:n.79+24253T>C
XR_943146.1:n.552-3002A>G
XR_001744423.1:n.606-3002A>G
XR_001744424.1:n.79+24253T>C