Canonical Allele Identifier: CA2735679572

Gene: CYP4F22

Linked Data

• dbSNP Id: rs2144533198

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540735G>A , CM000681.2:g.15540735G>A	GRCh38
NC_000019.9:g.15651546G>A , CM000681.1:g.15651546G>A	GRCh37
NC_000019.8:g.15512546G>A	NCBI36
NG_007987.1:g.37211G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+18G>A MANE Select	ENSP00000269703.1:n.939+18G>A
ENST00000269703.7:c.939+18G>A	ENSP00000269703.1:n.939+18G>A
ENST00000601005.2:c.939+18G>A	ENSP00000469866.1:n.939+18G>A
NM_173483.3:c.939+18G>A	NP_775754.2:n.939+18G>A
XM_011527692.1:c.939+18G>A	XP_011525994.1:n.939+18G>A
XM_011527693.1:c.939+18G>A	XP_011525995.1:n.939+18G>A
XM_011527692.2:c.939+18G>A	XP_011525994.1:n.939+18G>A
XM_011527693.2:c.939+18G>A	XP_011525995.1:n.939+18G>A
NM_173483.4:c.939+18G>A MANE Select	NP_775754.2:n.939+18G>A