Canonical Allele Identifier: CA619266149

Gene: FAH

Linked Data

• dbSNP Id: rs1238699727
• gnomAD v2: 15-80444967-G-T
• gnomAD v3: 15-80152625-G-T
• gnomAD v4: 15-80152625-G-T
• MyVariant Identifiers: chr15:g.80444967G>T (hg19) ; chr15:g.80152625G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80152625G>T , CM000677.2:g.80152625G>T	GRCh38
NC_000015.9:g.80444967G>T , CM000677.1:g.80444967G>T	GRCh37
NC_000015.8:g.78232022G>T	NCBI36
NG_012833.1:g.4627G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558022.5:c.-30+80G>T	ENSP00000453152.1:n.-30+80G>T