Canonical Allele Identifier: CA1838661485
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21035308G>A , CM000671.2:g.21035308G>A GRCh38
NC_000009.11:g.21035307G>A , CM000671.1:g.21035307G>A GRCh37
NC_000009.10:g.21025307G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929514.1:n.1210+1812G>A
XR_001746633.1:n.1142+2657G>A
XR_929514.2:n.1276+1812G>A