Canonical Allele Identifier: CA1677170104
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160668797A= , CM000668.2:g.160668797A= GRCh38
NC_000006.11:g.161089829A= , CM000668.1:g.161089829A= GRCh37
NC_000006.10:g.161009819A= NCBI36
NG_016147.1:g.2579T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000452651.1:n.115-2424T=