Canonical Allele Identifier: CA505872552

Gene: CYP4F2

Linked Data

• dbSNP Id: rs1335939544
• gnomAD v2: 19-16008308-G-A
• gnomAD v4: 19-15897498-G-A
• MyVariant Identifiers: chr19:g.16008308G>A (hg19) ; chr19:g.15897498G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15897498G>A , CM000681.2:g.15897498G>A	GRCh38
NC_000019.9:g.16008308G>A , CM000681.1:g.16008308G>A	GRCh37
NC_000019.8:g.15869308G>A	NCBI36
NG_007971.2:g.5577C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000221700.11:c.114C>T MANE Select	ENSP00000221700.3:p.Thr38=
ENST00000011989.11:c.114C>T	ENSP00000011989.8:p.Thr38=
ENST00000221700.10:c.114C>T	ENSP00000221700.3:p.Thr38=
ENST00000392846.7:n.49+528C>T
ENST00000586927.2:c.114C>T	ENSP00000465514.1:p.Thr38=
ENST00000587671.2:c.114C>T	ENSP00000467443.2:p.Thr38=
ENST00000608168.1:n.167C>T
NM_001082.4:c.114C>T	NP_001073.3:p.Thr38=
NM_001082.5:c.114C>T MANE Select	NP_001073.3:p.Thr38=