Canonical Allele Identifier: CA2504991843
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2800416G>A , CM000686.2:g.2800416G>A GRCh38
NC_000024.9:g.2668457G>A , CM000686.1:g.2668457G>A GRCh37
NC_000024.8:g.2728457G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000679518.1:n.106+25677G>A
ENST00000681787.1:n.106+25677G>A
ENST00000681940.1:n.106+25677G>A