Canonical Allele Identifier: CA274036974

Gene: FAH

Linked Data

• dbSNP Id: rs1009720145
• gnomAD v3: 15-80186128-A-G
• gnomAD v4: 15-80186128-A-G
• MyVariant Identifiers: chr15:g.80478470A>G (hg19) ; chr15:g.80186128A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80186128A>G , CM000677.2:g.80186128A>G	GRCh38
NC_000015.9:g.80478470A>G , CM000677.1:g.80478470A>G	GRCh37
NC_000015.8:g.78265525A>G	NCBI36
NG_012833.1:g.38130A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682012.1:n.1270-2A>G
ENST00000561421.6:c.1181-2A>G MANE Select	ENSP00000453347.2:n.1181-2A>G
ENST00000646551.1:n.2795-2A>G
ENST00000261755.9:c.1181-2A>G	ENSP00000261755.5:n.1181-2A>G
ENST00000407106.5:c.1181-2A>G	ENSP00000385080.1:n.1181-2A>G
ENST00000539156.5:c.971-2A>G	ENSP00000454271.1:n.971-2A>G
ENST00000559217.1:n.398-2A>G
ENST00000561421.5:c.1181-2A>G	ENSP00000453347.1:n.1181-2A>G
NM_000137.2:c.1181-2A>G	NP_000128.1:n.1181-2A>G
XM_024449872.1:c.1181-2A>G	XP_024305640.1:n.1181-2A>G
NM_000137.4:c.1181-2A>G MANE Select	NP_000128.1:n.1181-2A>G
NM_001374377.1:c.1181-2A>G	NP_001361306.1:n.1181-2A>G
NM_001374380.1:c.1181-2A>G	NP_001361309.1:n.1181-2A>G