Canonical Allele Identifier: CA1138669506
Gene:

Linked Data

dbSNP Id: rs2051130258

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2800443G>A , CM000686.2:g.2800443G>A GRCh38
NC_000024.9:g.2668484G>A , CM000686.1:g.2668484G>A GRCh37
NC_000024.8:g.2728484G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000679518.1:n.106+25704G>A
ENST00000681787.1:n.106+25704G>A
ENST00000681940.1:n.106+25704G>A