Canonical Allele Identifier: CA1246001929
Gene: GEMIN6 HGNC NCBI

Linked Data

dbSNP Id: rs1558618215

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38753119C>T , CM000664.2:g.38753119C>T GRCh38
NC_000002.11:g.38980261C>T , CM000664.1:g.38980261C>T GRCh37
NC_000002.10:g.38833765C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000409011.5:c.-281+1301C>T ENSP00000387191.1:n.-281+1301C>T