Canonical Allele Identifier: CA1677169864
Gene:

Linked Data

dbSNP Id: rs1780347364

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160668427T>A , CM000668.2:g.160668427T>A GRCh38
NC_000006.11:g.161089459T>A , CM000668.1:g.161089459T>A GRCh37
NC_000006.10:g.161009449T>A NCBI36
NG_016147.1:g.2949A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000452651.1:n.115-2054A>T