Canonical Allele Identifier: CA1677170011
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160668689T= , CM000668.2:g.160668689T= GRCh38
NC_000006.11:g.161089721T= , CM000668.1:g.161089721T= GRCh37
NC_000006.10:g.161009711T= NCBI36
NG_016147.1:g.2687A=

Transcript Alleles

HGVS Amino-acid change
ENST00000452651.1:n.115-2316A=