Canonical Allele Identifier: CA2734957233
Gene:

Linked Data

dbSNP Id: rs2144835127

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756583C>T , CM000680.2:g.31756583C>T GRCh38
NC_000018.9:g.29336546C>T , CM000680.1:g.29336546C>T GRCh37
NC_000018.8:g.27590544C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935338.1:n.66-5556C>T