Canonical Allele Identifier: CA26882042
Gene: F3 HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.94536311T>C
GRCh37 chr1:g.95001867T>C
gnomAD v2:
1:95001867 T / C
gnomAD v3:
1:94536311 T / C
gnomAD v4:
chr1-94536311-T-C
Joint Max Group AF 0.05219379 (NFE)
Genomes Max Group AF 0.05481968 (NFE)
Exomes Max Group AF 0.05147161 (NFE)
dbSNP:
3917643
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94536311T>C , CM000663.2:g.94536311T>C GRCh38
NC_000001.10:g.95001867T>C , CM000663.1:g.95001867T>C GRCh37
NC_000001.9:g.94774455T>C NCBI36
NG_029366.1:g.10547A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000334047.12:c.213-147A>G MANE Select ENSP00000334145.7:n.213-147A>G
ENST00000334047.11:c.213-147A>G ENSP00000334145.7:n.213-147A>G
ENST00000370207.4:c.213-147A>G ENSP00000359226.4:n.213-147A>G
ENST00000480356.1:n.831-147A>G
NM_001178096.1:c.213-147A>G NP_001171567.1:n.213-147A>G
NM_001993.4:c.213-147A>G NP_001984.1:n.213-147A>G
NM_001993.5:c.213-147A>G MANE Select NP_001984.1:n.213-147A>G
NM_001178096.2:c.213-147A>G NP_001171567.1:n.213-147A>G
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