Canonical Allele Identifier: CA136926547
Gene: GPSM3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1294559
ClinVar RCV Id: RCV001720463
dbSNP Id: rs204989
gnomAD v2: 6-32161852-G-A
gnomAD v3: 6-32194075-G-A
gnomAD v4: 6-32194075-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32194075G>A , CM000668.2:g.32194075G>A GRCh38
NC_000006.11:g.32161852G>A , CM000668.1:g.32161852G>A GRCh37
NC_000006.10:g.32269830G>A NCBI36
NG_028190.1:g.34993C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000375043.3:c.-102+235C>T ENSP00000364183.3:n.-102+235C>T
NM_022107.1:c.-102+235C>T NP_071390.1:n.-102+235C>T
NM_022107.2:c.-102+235C>T NP_071390.1:n.-102+235C>T
NM_022107.3:c.-102+235C>T NP_071390.1:n.-102+235C>T