Canonical Allele Identifier: CA305909986

Gene: CYP4F2

Linked Data

• dbSNP Id: rs781254717
• gnomAD v4: 19-15897603-C-G
• MyVariant Identifiers: chr19:g.16008413C>G (hg19) ; chr19:g.15897603C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15897603C>G , CM000681.2:g.15897603C>G	GRCh38
NC_000019.9:g.16008413C>G , CM000681.1:g.16008413C>G	GRCh37
NC_000019.8:g.15869413C>G	NCBI36
NG_007971.2:g.5472G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.9G>C MANE Select	ENSP00000221700.3:p.Gln3His
ENST00000011989.11:c.9G>C	ENSP00000011989.8:p.Gln3His
ENST00000221700.10:c.9G>C	ENSP00000221700.3:p.Gln3His
ENST00000392846.7:n.49+423G>C
ENST00000586927.2:c.9G>C	ENSP00000465514.1:p.Gln3His
ENST00000587671.2:c.9G>C	ENSP00000467443.2:p.Gln3His
ENST00000608168.1:n.62G>C
NM_001082.4:c.9G>C	NP_001073.3:p.Gln3His
NM_001082.5:c.9G>C MANE Select	NP_001073.3:p.Gln3His