Canonical Allele Identifier: CA2672446523
Gene: FGA HGNC NCBI

Linked Data

gnomAD v4: 4-154589077-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154589077T>G , CM000666.2:g.154589077T>G GRCh38
NC_000004.11:g.155510229T>G , CM000666.1:g.155510229T>G GRCh37
NC_000004.10:g.155729679T>G NCBI36
NG_008832.1:g.6669A>C , LRG_557:g.6669A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000651975.2:c.181-101A>C ENSP00000498441.1:n.181-101A>C
ENST00000403106.8:c.181-101A>C MANE Select ENSP00000385981.3:n.181-101A>C
ENST00000651975.1:c.181-101A>C ENSP00000498441.1:n.181-101A>C
ENST00000302053.7:c.181-101A>C ENSP00000306361.3:n.181-101A>C
ENST00000403106.7:c.181-101A>C ENSP00000385981.3:n.181-101A>C
ENST00000622532.1:c.181-101A>C ENSP00000478487.1:n.181-101A>C
NM_000508.3:c.181-101A>C , LRG_557t1:c.181-101A>C NP_000499.1:n.181-101A>C
NM_021871.2:c.181-101A>C , LRG_557t2:c.181-101A>C NP_068657.1:n.181-101A>C
NM_000508.4:c.181-101A>C NP_000499.1:n.181-101A>C
NM_021871.3:c.181-101A>C NP_068657.1:n.181-101A>C
NM_021871.4:c.181-101A>C MANE Select NP_068657.1:n.181-101A>C
NM_000508.5:c.181-101A>C NP_000499.1:n.181-101A>C
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