Canonical Allele Identifier: CA1096188204

Gene:

Linked Data

• dbSNP Id: rs1778859370
• gnomAD v3: 6-155812712-T-C
• gnomAD v4: 6-155812712-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.155812712T>C , CM000668.2:g.155812712T>C	GRCh38
NC_000006.11:g.156133846T>C , CM000668.1:g.156133846T>C	GRCh37
NC_000006.10:g.156175538T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_943142.1:n.79+19293T>C
XR_943146.1:n.645-673A>G
XR_001744423.1:n.699-673A>G
XR_001744424.1:n.79+19293T>C