Canonical Allele Identifier: CA994271
Gene: GSTM1 HGNC NCBI
GSTM2 HGNC NCBI
COSMIC:
COSN6502289 (not active)
COSN8635314 (not active)
MyVariant.info:
GRCh38 chr1:g.109689155G>A
GRCh37 chr1:g.110231777G>A
gnomAD v2:
1:110231777 G / A
gnomAD v3:
1:109689155 G / A
gnomAD v4:
chr1-109689155-G-A
Joint Max Group AF 0.62499542 (EAS)
Genomes Max Group AF 0.54904291 (EAS)
Exomes Max Group AF 0.63117536 (EAS)
dbSNP:
4147565
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109689155G>A , CM000663.2:g.109689155G>A GRCh38
NC_000001.10:g.110231777G>A , CM000663.1:g.110231777G>A GRCh37
NC_000001.9:g.110033300G>A NCBI36
NG_009246.1:g.6360G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309851.10:c.259+26G>A (GSTM1) MANE Select ENSP00000311469.5:n.259+26G>A
ENST00000309851.9:c.259+26G>A (GSTM1) ENSP00000311469.5:n.259+26G>A
ENST00000349334.7:c.259+26G>A (GSTM1) ENSP00000234981.4:n.259+26G>A
ENST00000369819.2:c.259+26G>A (GSTM1) ENSP00000358834.2:n.259+26G>A
ENST00000369823.6:c.316+26G>A (GSTM1) ENSP00000358838.2:n.316+26G>A
ENST00000369831.6:c.567+17572G>A (GSTM2) ENSP00000358846.2:n.567+17572G>A
ENST00000460717.7:c.*17+7321G>A (GSTM2) ENSP00000435910.2:n.*17+7321G>A
ENST00000476065.6:c.157+26G>A (GSTM1) ENSP00000456315.1:n.157+26G>A
ENST00000483399.6:c.178-70G>A (GSTM1) ENSP00000455929.1:n.178-70G>A
ENST00000490021.2:n.243+26G>A (GSTM1)
NM_000561.3:c.259+26G>A (GSTM1) NP_000552.2:n.259+26G>A
NM_146421.2:c.259+26G>A (GSTM1) NP_666533.1:n.259+26G>A
XM_005270782.3:c.157+26G>A (GSTM1) XP_005270839.1:n.157+26G>A
XM_005270783.3:c.-53-70G>A (GSTM1) XP_005270840.1:n.-53-70G>A
XM_005270782.5:c.157+26G>A (GSTM1) XP_005270839.1:n.157+26G>A
NM_000561.4:c.259+26G>A (GSTM1) MANE Select NP_000552.2:n.259+26G>A
NM_146421.3:c.259+26G>A (GSTM1) NP_666533.1:n.259+26G>A
Search 100 bp 5'
Search 100 bp 3'