Canonical Allele Identifier: CA1246001919
Gene: GEMIN6 HGNC NCBI

Linked Data

dbSNP Id: rs1668491775

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38753114T>C , CM000664.2:g.38753114T>C GRCh38
NC_000002.11:g.38980256T>C , CM000664.1:g.38980256T>C GRCh37
NC_000002.10:g.38833760T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000409011.5:c.-281+1296T>C ENSP00000387191.1:n.-281+1296T>C