Canonical Allele Identifier: CA1284431643
Gene:

Linked Data

dbSNP Id: rs1678946554

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122368839G>A , CM000664.2:g.122368839G>A GRCh38
NC_000002.11:g.123126415G>A , CM000664.1:g.123126415G>A GRCh37
NC_000002.10:g.122842885G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923278.1:n.556-24124G>A
XR_001739684.1:n.556-24124G>A