Canonical Allele Identifier: CA2360755165
Gene: SNTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443796C= , CM000682.2:g.33443796C= GRCh38
NC_000020.10:g.32031602C= , CM000682.1:g.32031602C= GRCh37
NC_000020.9:g.31495263C= NCBI36
NG_011622.1:g.5097G= , LRG_332:g.5097G=

Transcript Alleles

HGVS Amino-acid change
ENST00000217381.2:c.-176G= ENSP00000217381.2:n.-176G=
NM_003098.2:c.-176G= , LRG_332t1:c.-176G= NP_003089.1:n.-176G=
XM_005260517.1:c.-176G= XP_005260574.1:n.-176G=
XM_011529007.1:c.-176G= XP_011527309.1:n.-176G=
XM_011529008.1:c.-176G= XP_011527310.1:n.-176G=
XR_936612.1:n.58G=