Canonical Allele Identifier: CA1142045985
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.211379804C= , CM000663.2:g.211379804C= GRCh38
NC_000001.10:g.211553146C= , CM000663.1:g.211553146C= GRCh37
NC_000001.9:g.209619769C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001738446.1:n.291+2391G=