Canonical Allele Identifier: CA1677169873
Gene:

Linked Data

dbSNP Id: rs1780347579

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160668445T>G , CM000668.2:g.160668445T>G GRCh38
NC_000006.11:g.161089477T>G , CM000668.1:g.161089477T>G GRCh37
NC_000006.10:g.161009467T>G NCBI36
NG_016147.1:g.2931A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000452651.1:n.115-2072A>C