Canonical Allele Identifier: CA404579911

Gene: CYP4F2

Linked Data

• dbSNP Id: rs1197595235
• gnomAD v2: 19-16008328-C-T
• gnomAD v4: 19-15897518-C-T
• MyVariant Identifiers: chr19:g.16008328C>T (hg19) ; chr19:g.15897518C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15897518C>T , CM000681.2:g.15897518C>T	GRCh38
NC_000019.9:g.16008328C>T , CM000681.1:g.16008328C>T	GRCh37
NC_000019.8:g.15869328C>T	NCBI36
NG_007971.2:g.5557G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.94G>A MANE Select	ENSP00000221700.3:p.Ala32Thr
ENST00000011989.11:c.94G>A	ENSP00000011989.8:p.Ala32Thr
ENST00000221700.10:c.94G>A	ENSP00000221700.3:p.Ala32Thr
ENST00000392846.7:n.49+508G>A
ENST00000586927.2:c.94G>A	ENSP00000465514.1:p.Ala32Thr
ENST00000587671.2:c.94G>A	ENSP00000467443.2:p.Ala32Thr
ENST00000608168.1:n.147G>A
NM_001082.4:c.94G>A	NP_001073.3:p.Ala32Thr
NM_001082.5:c.94G>A MANE Select	NP_001073.3:p.Ala32Thr