Canonical Allele Identifier: CA2734203694
Gene: TSEN54 HGNC NCBI

Linked Data

dbSNP Id: rs2147003743
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516096G>A , CM000679.2:g.75516096G>A GRCh38
NC_000017.10:g.73512177G>A , CM000679.1:g.73512177G>A GRCh37
NC_000017.9:g.71023772G>A NCBI36
NG_013041.1:g.4569G>A
NG_033152.1:g.4488C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-373G>A ENSP00000406559.4:n.-373G>A
ENST00000679370.1:n.153G>A
ENST00000434205.7:c.-373G>A ENSP00000406559.3:n.-373G>A
XM_006721821.2:c.-538G>A XP_006721884.1:n.-538G>A
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