Canonical Allele Identifier: CA789376598
Gene: FGA HGNC NCBI

Linked Data

dbSNP Id: rs1210721316
MyVariant Identifiers: chr4:g.155504971T>C (hg19) chr4:g.154583819T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154583819T>C , CM000666.2:g.154583819T>C GRCh38
NC_000004.11:g.155504971T>C , CM000666.1:g.155504971T>C GRCh37
NC_000004.10:g.155724421T>C NCBI36
NG_008832.1:g.11927A>G , LRG_557:g.11927A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651975.2:c.*305A>G ENSP00000498441.1:n.*305A>G
ENST00000651975.1:c.*305A>G ENSP00000498441.1:n.*305A>G
ENST00000302053.7:c.*305A>G ENSP00000306361.3:n.*305A>G
NM_000508.3:c.*305A>G , LRG_557t1:c.*305A>G NP_000499.1:n.*305A>G
NM_000508.4:c.*305A>G NP_000499.1:n.*305A>G
NM_000508.5:c.*305A>G NP_000499.1:n.*305A>G
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