Canonical Allele Identifier: CA1677169913
Gene:

Linked Data

dbSNP Id: rs1582912334

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160668531G>C , CM000668.2:g.160668531G>C GRCh38
NC_000006.11:g.161089563G>C , CM000668.1:g.161089563G>C GRCh37
NC_000006.10:g.161009553G>C NCBI36
NG_016147.1:g.2845C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000452651.1:n.115-2158C>G