Canonical Allele Identifier: CA619268246

Gene: FAH

Linked Data

• dbSNP Id: rs1296431383
• gnomAD v2: 15-80460519-C-T
• gnomAD v4: 15-80168177-C-T
• MyVariant Identifiers: chr15:g.80460519C>T (hg19) ; chr15:g.80168177C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80168177C>T , CM000677.2:g.80168177C>T	GRCh38
NC_000015.9:g.80460519C>T , CM000677.1:g.80460519C>T	GRCh37
NC_000015.8:g.78247574C>T	NCBI36
NG_012833.1:g.20179C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682012.1:n.656C>T
ENST00000684569.1:n.598+28C>T
ENST00000561421.6:c.553+28C>T MANE Select	ENSP00000453347.2:n.553+28C>T
ENST00000646551.1:n.2180+28C>T
ENST00000261755.9:c.553+28C>T	ENSP00000261755.5:n.553+28C>T
ENST00000407106.5:c.553+28C>T	ENSP00000385080.1:n.553+28C>T
ENST00000539156.5:c.343+28C>T	ENSP00000454271.1:n.343+28C>T
ENST00000558514.1:n.99+28C>T
ENST00000558627.1:n.481+28C>T
ENST00000561421.5:c.553+28C>T	ENSP00000453347.1:n.553+28C>T
NM_000137.2:c.553+28C>T	NP_000128.1:n.553+28C>T
XM_024449872.1:c.553+28C>T	XP_024305640.1:n.553+28C>T
NM_000137.4:c.553+28C>T MANE Select	NP_000128.1:n.553+28C>T
NM_001374377.1:c.553+28C>T	NP_001361306.1:n.553+28C>T
NM_001374380.1:c.553+28C>T	NP_001361309.1:n.553+28C>T