Canonical Allele Identifier: CA100033015

Gene: FGF5

Linked Data

• dbSNP Id: rs1021434528
• gnomAD v3: 4-80286778-A-G
• gnomAD v4: 4-80286778-A-G
• MyVariant Identifiers: chr4:g.81207932A>G (hg19) ; chr4:g.80286778A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80286778A>G , CM000666.2:g.80286778A>G	GRCh38
NC_000004.11:g.81207932A>G , CM000666.1:g.81207932A>G	GRCh37
NC_000004.10:g.81426956A>G	NCBI36
NG_029501.1:g.25191A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312465.12:c.*106A>G MANE Select	ENSP00000311697.7:n.*106A>G
ENST00000312465.11:c.*106A>G	ENSP00000311697.7:n.*106A>G
ENST00000456523.3:c.*437A>G	ENSP00000398353.3:n.*437A>G
ENST00000503413.1:n.862A>G
ENST00000507780.1:c.342+11766A>G	ENSP00000423903.1:n.342+11766A>G
NM_001291812.1:c.*106A>G	NP_001278741.1:n.*106A>G
NM_004464.3:c.*106A>G	NP_004455.2:n.*106A>G
NM_033143.2:c.*437A>G	NP_149134.1:n.*437A>G
NM_001291812.2:c.*106A>G	NP_001278741.1:n.*106A>G
NM_004464.4:c.*106A>G MANE Select	NP_004455.2:n.*106A>G