Canonical Allele Identifier: CA631975505

Gene: CYP4F2

Linked Data

• dbSNP Id: rs1176852124
• gnomAD v2: 19-16007983-T-C
• gnomAD v3: 19-15897173-T-C
• gnomAD v4: 19-15897173-T-C
• MyVariant Identifiers: chr19:g.16007983T>C (hg19) ; chr19:g.15897173T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15897173T>C , CM000681.2:g.15897173T>C	GRCh38
NC_000019.9:g.16007983T>C , CM000681.1:g.16007983T>C	GRCh37
NC_000019.8:g.15868983T>C	NCBI36
NG_007971.2:g.5902A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.198+241A>G MANE Select	ENSP00000221700.3:n.198+241A>G
ENST00000011989.11:c.198+241A>G	ENSP00000011989.8:n.198+241A>G
ENST00000221700.10:c.198+241A>G	ENSP00000221700.3:n.198+241A>G
ENST00000392846.7:n.49+853A>G
ENST00000586927.2:c.198+241A>G	ENSP00000465514.1:n.198+241A>G
ENST00000587671.2:c.198+241A>G	ENSP00000467443.2:n.198+241A>G
ENST00000608168.1:n.251+241A>G
NM_001082.4:c.198+241A>G	NP_001073.3:n.198+241A>G
NM_001082.5:c.198+241A>G MANE Select	NP_001073.3:n.198+241A>G