Canonical Allele Identifier: CA54648337
Gene:

Linked Data

dbSNP Id: rs868773609

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120332111G>T , CM000664.2:g.120332111G>T GRCh38
NC_000002.11:g.121089687G>T , CM000664.1:g.121089687G>T GRCh37
NC_000002.10:g.120806157G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011512307.1:n.141+3305G>T XP_011510609.1:p.=