Canonical Allele Identifier: CA294075207
Gene: TSEN54 HGNC NCBI

Linked Data

dbSNP Id: rs542549656

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516147G>A , CM000679.2:g.75516147G>A GRCh38
NC_000017.10:g.73512228G>A , CM000679.1:g.73512228G>A GRCh37
NC_000017.9:g.71023823G>A NCBI36
NG_013041.1:g.4620G>A
NG_033152.1:g.4437C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-322G>A ENSP00000406559.4:n.-322G>A
ENST00000679370.1:n.204G>A
ENST00000434205.7:c.-322G>A ENSP00000406559.3:n.-322G>A
XM_006721821.2:c.-487G>A XP_006721884.1:n.-487G>A