Canonical Allele Identifier: CA11148164
Gene: TOGARAM2 HGNC NCBI
MyVariant.info:
GRCh38 chr2:g.29057895C>T
GRCh37 chr2:g.29280761C>T
gnomAD v2:
2:29280761 C / T
gnomAD v3:
2:29057895 C / T
gnomAD v4:
chr2-29057895-C-T
Joint Max Group AF 0.30181124 (MID)
Genomes Max Group AF 0.29284922 (NFE)
Exomes Max Group AF 0.029613 (NFE)
dbSNP:
882632
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29057895C>T , CM000664.2:g.29057895C>T GRCh38
NC_000002.11:g.29280761C>T , CM000664.1:g.29280761C>T GRCh37
NC_000002.10:g.29134265C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000379558.4:c.*5802C>T ENSP00000368876.3:n.*5802C>T
NM_001321538.2:c.*5802C>T NP_001308467.1:n.*5802C>T
NM_001321539.2:c.*5802C>T NP_001308468.1:n.*5802C>T
NM_199280.3:c.*5802C>T NP_954974.2:n.*5802C>T
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