Canonical Allele Identifier: CA1619157137
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31439986A= , CM000668.2:g.31439986A= GRCh38
NC_000006.11:g.31407763A= , CM000668.1:g.31407763A= GRCh37
NC_000006.10:g.31515742A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926694.1:n.121T=