Canonical Allele Identifier: CA2639834508
Gene: TSEN54 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516373G>T , CM000679.2:g.75516373G>T GRCh38
NC_000017.10:g.73512454G>T , CM000679.1:g.73512454G>T GRCh37
NC_000017.9:g.71024049G>T NCBI36
NG_013041.1:g.4846G>T
NG_033152.1:g.4211C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-96G>T ENSP00000406559.4:n.-96G>T
ENST00000679370.1:n.430G>T
ENST00000434205.7:c.-96G>T ENSP00000406559.3:n.-96G>T
XM_006721821.2:c.-261G>T XP_006721884.1:n.-261G>T