Canonical Allele Identifier: CA1663384865
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.129895365A= , CM000668.2:g.129895365A= GRCh38
NC_000006.11:g.130216510A= , CM000668.1:g.130216510A= GRCh37
NC_000006.10:g.130258203A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_942986.1:n.355+7292A=
XR_942986.2:n.355+7292A=