Canonical Allele Identifier: CA108763214
Gene: FGA HGNC NCBI
MyVariant.info:
GRCh38 chr4:g.154589162A>G
GRCh37 chr4:g.155510314A>G
gnomAD v2:
4:155510314 A / G
gnomAD v3:
4:154589162 A / G
gnomAD v4:
chr4-154589162-A-G
Joint Max Group AF 0.19809904 (EAS)
Genomes Max Group AF 0.19809904 (EAS)
ClinVar RCV:
RCV001693192
ClinVar Variation:
1279619
dbSNP:
2070016
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154589162A>G , CM000666.2:g.154589162A>G GRCh38
NC_000004.11:g.155510314A>G , CM000666.1:g.155510314A>G GRCh37
NC_000004.10:g.155729764A>G NCBI36
NG_008832.1:g.6584T>C , LRG_557:g.6584T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651975.2:c.181-186T>C ENSP00000498441.1:n.181-186T>C
ENST00000403106.8:c.181-186T>C MANE Select ENSP00000385981.3:n.181-186T>C
ENST00000651975.1:c.181-186T>C ENSP00000498441.1:n.181-186T>C
ENST00000302053.7:c.181-186T>C ENSP00000306361.3:n.181-186T>C
ENST00000403106.7:c.181-186T>C ENSP00000385981.3:n.181-186T>C
ENST00000622532.1:c.181-186T>C ENSP00000478487.1:n.181-186T>C
NM_000508.3:c.181-186T>C , LRG_557t1:c.181-186T>C NP_000499.1:n.181-186T>C
NM_021871.2:c.181-186T>C , LRG_557t2:c.181-186T>C NP_068657.1:n.181-186T>C
NM_000508.4:c.181-186T>C NP_000499.1:n.181-186T>C
NM_021871.3:c.181-186T>C NP_068657.1:n.181-186T>C
NM_021871.4:c.181-186T>C MANE Select NP_068657.1:n.181-186T>C
NM_000508.5:c.181-186T>C NP_000499.1:n.181-186T>C
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