Canonical Allele Identifier: CA6038593
Gene: TMEM258 HGNC NCBI
MyVariant.info:
GRCh38 chr11:g.61792609G>A
GRCh37 chr11:g.61560081G>A
gnomAD v2:
11:61560081 G / A
gnomAD v3:
11:61792609 G / A
gnomAD v4:
chr11-61792609-G-A
Joint Max Group AF 0.58952899 (AMR)
Genomes Max Group AF 0.53149537 (EAS)
Exomes Max Group AF 0.63155606 (AMR)
dbSNP:
174538
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61792609G>A , CM000673.2:g.61792609G>A GRCh38
NC_000011.9:g.61560081G>A , CM000673.1:g.61560081G>A GRCh37
NC_000011.8:g.61316657G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000535297.1:c.-51C>T ENSP00000437809.1:n.-51C>T
ENST00000537328.5:c.-51C>T ENSP00000443216.1:n.-51C>T
ENST00000543510.1:c.-1159C>T ENSP00000443836.1:n.-1159C>T
NM_014206.3:c.-51C>T NP_055021.1:n.-51C>T
Search 100 bp 5'
Search 100 bp 3'