Canonical Allele Identifier: CA1369169925
Gene:

Linked Data

dbSNP Id: rs2041753968

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.61428238C>T , CM000665.2:g.61428238C>T GRCh38
NC_000003.11:g.61413912C>T , CM000665.1:g.61413912C>T GRCh37
NC_000003.10:g.61388952C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940892.1:n.164+276G>A
XR_940893.1:n.164+276G>A
XR_001740725.1:n.202+276G>A
XR_940892.2:n.202+276G>A