Canonical Allele Identifier: CA1319876350
Gene:

Linked Data

dbSNP Id: rs1701760085

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.198767782T>C , CM000664.2:g.198767782T>C GRCh38
NC_000002.11:g.199632506T>C , CM000664.1:g.199632506T>C GRCh37
NC_000002.10:g.199340751T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923758.1:n.72+4477A>G
XR_923759.1:n.72+4477A>G
XR_923760.1:n.72+4477A>G
XR_923759.2:n.72+4477A>G
XR_923760.2:n.72+4477A>G