Canonical Allele Identifier: CA775072440
Gene: TSEN54 HGNC NCBI

Linked Data

dbSNP Id: rs1173590391

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516223G>T , CM000679.2:g.75516223G>T GRCh38
NC_000017.10:g.73512304G>T , CM000679.1:g.73512304G>T GRCh37
NC_000017.9:g.71023899G>T NCBI36
NG_013041.1:g.4696G>T
NG_033152.1:g.4361C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-246G>T ENSP00000406559.4:n.-246G>T
ENST00000679370.1:n.280G>T
ENST00000434205.7:c.-246G>T ENSP00000406559.3:n.-246G>T
XM_006721821.2:c.-411G>T XP_006721884.1:n.-411G>T