Canonical Allele Identifier: CA1096565020
Gene:

Linked Data

dbSNP Id: rs1398228621

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160668490C>G , CM000668.2:g.160668490C>G GRCh38
NC_000006.11:g.161089522C>G , CM000668.1:g.161089522C>G GRCh37
NC_000006.10:g.161009512C>G NCBI36
NG_016147.1:g.2886G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000452651.1:n.115-2117G>C