Canonical Allele Identifier: CA632130234

Gene: CYP4F2

Linked Data

• dbSNP Id: rs1175183245
• gnomAD v2: 19-15990363-C-G
• gnomAD v3: 19-15879553-C-G
• gnomAD v4: 19-15879553-C-G
• MyVariant Identifiers: chr19:g.15990363C>G (hg19) ; chr19:g.15879553C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15879553C>G , CM000681.2:g.15879553C>G	GRCh38
NC_000019.9:g.15990363C>G , CM000681.1:g.15990363C>G	GRCh37
NC_000019.8:g.15851363C>G	NCBI36
NG_007971.2:g.23522G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.1314+51G>C MANE Select	ENSP00000221700.3:n.1314+51G>C
ENST00000011989.11:c.1314+51G>C	ENSP00000011989.8:n.1314+51G>C
ENST00000221700.10:c.1314+51G>C	ENSP00000221700.3:n.1314+51G>C
ENST00000392846.7:n.1257+51G>C
ENST00000589654.2:c.103-125G>C
NM_001082.4:c.1314+51G>C	NP_001073.3:n.1314+51G>C
NM_001082.5:c.1314+51G>C MANE Select	NP_001073.3:n.1314+51G>C