Canonical Allele Identifier: CA1250988213
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.53010182G= , CM000664.2:g.53010182G= GRCh38
NC_000002.11:g.53237320G= , CM000664.1:g.53237320G= GRCh37
NC_000002.10:g.53090824G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959384.1:n.124-100158C=