Canonical Allele Identifier: CA993965965

Gene: CYP4F2

Linked Data

• dbSNP Id: rs1599359425
• gnomAD v3: 19-15897713-T-C
• gnomAD v4: 19-15897713-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15897713T>C , CM000681.2:g.15897713T>C	GRCh38
NC_000019.9:g.16008523T>C , CM000681.1:g.16008523T>C	GRCh37
NC_000019.8:g.15869523T>C	NCBI36
NG_007971.2:g.5362A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.-1-101A>G MANE Select	ENSP00000221700.3:n.-1-101A>G
ENST00000011989.11:c.-1-101A>G	ENSP00000011989.8:n.-1-101A>G
ENST00000221700.10:c.-1-101A>G	ENSP00000221700.3:n.-1-101A>G
ENST00000392846.7:n.49+313A>G
ENST00000586927.2:c.-102A>G	ENSP00000465514.1:n.-102A>G
ENST00000587671.2:c.-1-101A>G	ENSP00000467443.2:n.-1-101A>G
ENST00000608168.1:n.53-101A>G
NM_001082.4:c.-1-101A>G	NP_001073.3:n.-1-101A>G
NM_001082.5:c.-1-101A>G MANE Select	NP_001073.3:n.-1-101A>G