Canonical Allele Identifier: CA803778398
Gene:

Linked Data

dbSNP Id: rs1454337649

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.129386946T>G , CM000667.2:g.129386946T>G GRCh38
NC_000005.9:g.128722639T>G , CM000667.1:g.128722639T>G GRCh37
NC_000005.8:g.128750538T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427770.2:n.163-1502T>G
XR_948774.1:n.235-5705T>G
XR_001742463.1:n.4089-1502T>G
XR_001742464.1:n.2019-5705T>G
XR_001742465.1:n.401-1502T>G
XR_427770.3:n.337-1502T>G