Canonical Allele Identifier: CA11032601
Gene: TEX41 HGNC NCBI
MyVariant.info:
GRCh38 chr2:g.145043894T>C
GRCh37 chr2:g.145801461T>C
gnomAD v2:
2:145801461 T / C
gnomAD v3:
2:145043894 T / C
gnomAD v4:
chr2-145043894-T-C
Joint Max Group AF 0.80457891 (AFR)
Genomes Max Group AF 0.80457891 (AFR)
Exomes Max Group AF 0.13663143 (NFE)
dbSNP:
2252641
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.145043894T>C , CM000664.2:g.145043894T>C GRCh38
NC_000002.11:g.145801461T>C , CM000664.1:g.145801461T>C GRCh37
NC_000002.10:g.145517931T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033870.2:n.464-26926T>C
XR_923411.1:n.200+20621T>C
XR_923410.2:n.1051+20621T>C
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