Canonical Allele Identifier: CA2273295135
Gene:

Linked Data

dbSNP Id: rs1905462103

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.70831989G>T , CM000679.2:g.70831989G>T GRCh38
NC_000017.10:g.68828130G>T , CM000679.1:g.68828130G>T GRCh37
NC_000017.9:g.66339725G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934956.1:n.62+3225C>A
XR_934956.2:n.114+3225C>A