Canonical Allele Identifier: CA716075982

Gene: FAH

Linked Data

• dbSNP Id: rs1485039016
• gnomAD v4: 15-80177492-T-C
• MyVariant Identifiers: chr15:g.80469834T>C (hg19) ; chr15:g.80177492T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80177492T>C , CM000677.2:g.80177492T>C	GRCh38
NC_000015.9:g.80469834T>C , CM000677.1:g.80469834T>C	GRCh37
NC_000015.8:g.78256889T>C	NCBI36
NG_012833.1:g.29494T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682012.1:n.1003-45T>C
ENST00000561421.6:c.914-45T>C MANE Select	ENSP00000453347.2:n.914-45T>C
ENST00000646551.1:n.2528-45T>C
ENST00000261755.9:c.914-45T>C	ENSP00000261755.5:n.914-45T>C
ENST00000407106.5:c.914-45T>C	ENSP00000385080.1:n.914-45T>C
ENST00000539156.5:c.704-45T>C	ENSP00000454271.1:n.704-45T>C
ENST00000559217.1:n.86T>C
ENST00000561353.2:c.12-45T>C
ENST00000561421.5:c.914-45T>C	ENSP00000453347.1:n.914-45T>C
NM_000137.2:c.914-45T>C	NP_000128.1:n.914-45T>C
XM_024449872.1:c.914-45T>C	XP_024305640.1:n.914-45T>C
NM_000137.4:c.914-45T>C MANE Select	NP_000128.1:n.914-45T>C
NM_001374377.1:c.914-45T>C	NP_001361306.1:n.914-45T>C
NM_001374380.1:c.914-45T>C	NP_001361309.1:n.914-45T>C