Canonical Allele Identifier: CA223269378
Gene: MS4A2 HGNC NCBI
MyVariant.info:
GRCh38 chr11:g.60088555T>C
GRCh37 chr11:g.59856028T>C
gnomAD v2:
11:59856028 T / C
gnomAD v3:
11:60088555 T / C
gnomAD v4:
chr11-60088555-T-C
Joint Max Group AF 0.53504976 (SAS)
Genomes Max Group AF 0.52948576 (SAS)
Exomes Max Group AF 0.5342383 (SAS)
dbSNP:
1441586
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.60088555T>C , CM000673.2:g.60088555T>C GRCh38
NC_000011.9:g.59856028T>C , CM000673.1:g.59856028T>C GRCh37
NC_000011.8:g.59612604T>C NCBI36
NG_016014.1:g.4892T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000524868.1:c.-123T>C ENSP00000433311.1:n.-123T>C
XM_005273846.3:c.-102T>C XP_005273903.1:n.-102T>C
XM_011544850.1:c.-16-195T>C XP_011543152.1:n.-16-195T>C
XM_005273846.4:c.-102T>C XP_005273903.1:n.-102T>C
XM_011544850.2:c.-16-195T>C XP_011543152.1:n.-16-195T>C
XM_017017362.1:c.-102T>C XP_016872851.1:n.-102T>C
Search 100 bp 5'
Search 100 bp 3'