Canonical Allele Identifier: CA1677169929
Gene:

Linked Data

dbSNP Id: rs1780349405

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160668570T>C , CM000668.2:g.160668570T>C GRCh38
NC_000006.11:g.161089602T>C , CM000668.1:g.161089602T>C GRCh37
NC_000006.10:g.161009592T>C NCBI36
NG_016147.1:g.2806A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000452651.1:n.115-2197A>G