Canonical Allele Identifier: CA404579881

Gene: CYP4F2

Linked Data

• MyVariant Identifiers: chr19:g.16008312C>G (hg19) ; chr19:g.15897502C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15897502C>G , CM000681.2:g.15897502C>G	GRCh38
NC_000019.9:g.16008312C>G , CM000681.1:g.16008312C>G	GRCh37
NC_000019.8:g.15869312C>G	NCBI36
NG_007971.2:g.5573G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000221700.11:c.110G>C MANE Select	ENSP00000221700.3:p.Trp37Ser
ENST00000011989.11:c.110G>C	ENSP00000011989.8:p.Trp37Ser
ENST00000221700.10:c.110G>C	ENSP00000221700.3:p.Trp37Ser
ENST00000392846.7:n.49+524G>C
ENST00000586927.2:c.110G>C	ENSP00000465514.1:p.Trp37Ser
ENST00000587671.2:c.110G>C	ENSP00000467443.2:p.Trp37Ser
ENST00000608168.1:n.163G>C
NM_001082.4:c.110G>C	NP_001073.3:p.Trp37Ser
NM_001082.5:c.110G>C MANE Select	NP_001073.3:p.Trp37Ser