Canonical Allele Identifier: CA786695578
Gene:

Linked Data

dbSNP Id: rs1320887029

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578344C>T , CM000666.2:g.12578344C>T GRCh38
NC_000004.11:g.12579968C>T , CM000666.1:g.12579968C>T GRCh37
NC_000004.10:g.12189066C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925406.1:n.106+30998G>A
XR_001741374.1:n.254+44311G>A
XR_925406.3:n.140+30998G>A