Canonical Allele Identifier: CA12068026
Gene: TIMD4 HGNC NCBI
COSMIC:
COSN20368410 (not active)
MyVariant.info:
GRCh38 chr5:g.156971158G>C
GRCh37 chr5:g.156398169G>C
gnomAD v2:
5:156398169 G / C
gnomAD v3:
5:156971158 G / C
gnomAD v4:
chr5-156971158-G-C
Joint Max Group AF 0.72506167 (EAS)
Genomes Max Group AF 0.72506167 (EAS)
dbSNP:
1501908
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.156971158G>C , CM000667.2:g.156971158G>C GRCh38
NC_000005.9:g.156398169G>C , CM000667.1:g.156398169G>C GRCh37
NC_000005.8:g.156330747G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011534693.1:c.-96+1085C>G XP_011532995.1:n.-96+1085C>G
Search 100 bp 5'
Search 100 bp 3'