Canonical Allele Identifier: CA535757854
Gene:

Linked Data

dbSNP Id: rs1308568921

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120332056A>G , CM000664.2:g.120332056A>G GRCh38
NC_000002.11:g.121089632A>G , CM000664.1:g.121089632A>G GRCh37
NC_000002.10:g.120806102A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011512307.1:c.141+3250A>G XP_011510609.1:n.141+3250A>G