Canonical Allele Identifier: CA1035827879
Gene:

Linked Data

dbSNP Id: rs1049850175

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122884063G>T , CM000664.2:g.122884063G>T GRCh38
NC_000002.11:g.123641639G>T , CM000664.1:g.123641639G>T GRCh37
NC_000002.10:g.123358109G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923292.1:n.1125-879G>T
XR_001739692.1:n.1451-879G>T
XR_923292.2:n.1358-879G>T