Canonical Allele Identifier: CA305826025

Gene: CYP4F22

Linked Data

• dbSNP Id: rs1048185918
• gnomAD v2: 19-15651173-T-C
• gnomAD v3: 19-15540362-T-C
• gnomAD v4: 19-15540362-T-C
• MyVariant Identifiers: chr19:g.15651173T>C (hg19) ; chr19:g.15540362T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540362T>C , CM000681.2:g.15540362T>C	GRCh38
NC_000019.9:g.15651173T>C , CM000681.1:g.15651173T>C	GRCh37
NC_000019.8:g.15512173T>C	NCBI36
NG_007987.1:g.36838T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.672-88T>C MANE Select	ENSP00000269703.1:n.672-88T>C
ENST00000269703.7:c.672-88T>C	ENSP00000269703.1:n.672-88T>C
ENST00000601005.2:c.672-88T>C	ENSP00000469866.1:n.672-88T>C
NM_173483.3:c.672-88T>C	NP_775754.2:n.672-88T>C
XM_011527692.1:c.672-88T>C	XP_011525994.1:n.672-88T>C
XM_011527693.1:c.672-88T>C	XP_011525995.1:n.672-88T>C
XM_011527692.2:c.672-88T>C	XP_011525994.1:n.672-88T>C
XM_011527693.2:c.672-88T>C	XP_011525995.1:n.672-88T>C
NM_173483.4:c.672-88T>C MANE Select	NP_775754.2:n.672-88T>C