Canonical Allele Identifier: CA2275548146
Gene: TSEN54 HGNC NCBI

Linked Data

dbSNP Id: rs2053363272

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516288G>A , CM000679.2:g.75516288G>A GRCh38
NC_000017.10:g.73512369G>A , CM000679.1:g.73512369G>A GRCh37
NC_000017.9:g.71023964G>A NCBI36
NG_013041.1:g.4761G>A
NG_033152.1:g.4296C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-181G>A ENSP00000406559.4:n.-181G>A
ENST00000679370.1:n.345G>A
ENST00000434205.7:c.-181G>A ENSP00000406559.3:n.-181G>A
XM_006721821.2:c.-346G>A XP_006721884.1:n.-346G>A