Canonical Allele Identifier: CA1284674083
Gene:

Linked Data

dbSNP Id: rs1478913239

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122883904G>T , CM000664.2:g.122883904G>T GRCh38
NC_000002.11:g.123641480G>T , CM000664.1:g.123641480G>T GRCh37
NC_000002.10:g.123357950G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923292.1:n.1125-1038G>T
XR_001739692.1:n.1451-1038G>T
XR_923292.2:n.1358-1038G>T