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Canonical Allele Identifier:
CA358522685
Gene: FGA
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.154584311C>G , CM000666.2:g.154584311C>G
GRCh38
NC_000004.11:g.155505463C>G , CM000666.1:g.155505463C>G
GRCh37
NC_000004.10:g.155724913C>G
NCBI36
NG_008832.1:g.11435G>C , LRG_557:g.11435G>C
Transcript Alleles
HGVS
Amino-acid Change
ENST00000651975.2:c.2414G>C
ENSP00000498441.1:p.Gly805Ala
ENST00000651975.1:c.2414G>C
ENSP00000498441.1:p.Gly805Ala
ENST00000302053.7:c.2414G>C
ENSP00000306361.3:p.Gly805Ala
NM_000508.3:c.2414G>C , LRG_557t1:c.2414G>C
NP_000499.1:p.Gly805Ala
NM_000508.4:c.2414G>C
NP_000499.1:p.Gly805Ala
NM_000508.5:c.2414G>C
NP_000499.1:p.Gly805Ala
Search 100 bp 5'
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