Canonical Allele Identifier: CA1674885622
Gene:

Linked Data

dbSNP Id: rs1778855328

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812409A>C , CM000668.2:g.155812409A>C GRCh38
NC_000006.11:g.156133543A>C , CM000668.1:g.156133543A>C GRCh37
NC_000006.10:g.156175235A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+18990A>C
XR_943146.1:n.645-370T>G
XR_001744423.1:n.699-370T>G
XR_001744424.1:n.79+18990A>C