Canonical Allele Identifier: CA1283487615
Gene:

Linked Data

dbSNP Id: rs1690915827

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120332330A>G , CM000664.2:g.120332330A>G GRCh38
NC_000002.11:g.121089906A>G , CM000664.1:g.121089906A>G GRCh37
NC_000002.10:g.120806376A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011512307.1:c.141+3524A>G XP_011510609.1:n.141+3524A>G