Canonical Allele Identifier: CA10758089
Gene:

Linked Data

dbSNP Id: rs16840493

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240704176C>T , CM000663.2:g.240704176C>T GRCh38
NC_000001.10:g.240867476C>T , CM000663.1:g.240867476C>T GRCh37
NC_000001.9:g.238934099C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949320.1:n.74+5770G>A
XR_949320.2:n.124+5770G>A