Canonical Allele Identifier: CA1677170008
Gene:

Linked Data

dbSNP Id: rs1582912452

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160668686T>G , CM000668.2:g.160668686T>G GRCh38
NC_000006.11:g.161089718T>G , CM000668.1:g.161089718T>G GRCh37
NC_000006.10:g.161009708T>G NCBI36
NG_016147.1:g.2690A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000452651.1:n.115-2313A>C