Canonical Allele Identifier: CA2832471190
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160668626G>A , CM000668.2:g.160668626G>A GRCh38
NC_000006.11:g.161089658G>A , CM000668.1:g.161089658G>A GRCh37
NC_000006.10:g.161009648G>A NCBI36
NG_016147.1:g.2750C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000452651.1:n.115-2253C>T