Canonical Allele Identifier: CA821223656
Gene:

Linked Data

dbSNP Id: rs1299005091

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812610G>T , CM000668.2:g.155812610G>T GRCh38
NC_000006.11:g.156133744G>T , CM000668.1:g.156133744G>T GRCh37
NC_000006.10:g.156175436G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+19191G>T
XR_943146.1:n.645-571C>A
XR_001744423.1:n.699-571C>A
XR_001744424.1:n.79+19191G>T