Canonical Allele Identifier: CA631973745

Gene: CYP4F2

Linked Data

• dbSNP Id: rs1209738806
• gnomAD v2: 19-15990092-A-G
• gnomAD v3: 19-15879282-A-G
• gnomAD v4: 19-15879282-A-G
• MyVariant Identifiers: chr19:g.15990092A>G (hg19) ; chr19:g.15879282A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15879282A>G , CM000681.2:g.15879282A>G	GRCh38
NC_000019.9:g.15990092A>G , CM000681.1:g.15990092A>G	GRCh37
NC_000019.8:g.15851092A>G	NCBI36
NG_007971.2:g.23793T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.1397+64T>C MANE Select	ENSP00000221700.3:n.1397+64T>C
ENST00000011989.11:c.1397+64T>C	ENSP00000011989.8:n.1397+64T>C
ENST00000221700.10:c.1397+64T>C	ENSP00000221700.3:n.1397+64T>C
ENST00000392846.7:n.1340+64T>C
ENST00000589654.2:c.185+64T>C
NM_001082.4:c.1397+64T>C	NP_001073.3:n.1397+64T>C
NM_001082.5:c.1397+64T>C MANE Select	NP_001073.3:n.1397+64T>C