Canonical Allele Identifier: CA1674885854

Gene:

Linked Data

• dbSNP Id: rs1778858171

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.155812613A>G , CM000668.2:g.155812613A>G	GRCh38
NC_000006.11:g.156133747A>G , CM000668.1:g.156133747A>G	GRCh37
NC_000006.10:g.156175439A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943142.1:n.79+19194A>G
XR_943146.1:n.645-574T>C
XR_001744423.1:n.699-574T>C
XR_001744424.1:n.79+19194A>G