Allele Registry

SUSPENSION NOTICE:2024-08-07T19:00:00-0500 — 2024-09-25T08:00:00-0500
New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.

ALLELE REGISTRY - SERVICE INTERRUPTION2024-08-10T11:00:00-0500 — 2024-08-10T15:00:00-0500
The ClinGen Allele Registry will have an off-hours outage to perform maintenance tasks.
The outage will not take the entire interruption period.

ClinGen Allele Registry

Canonical Allele Identifier: CA632129610

Gene: CYP4F22 HGNC NCBI

Linked Data

dbSNP Id: rs1201665289

gnomAD v2: 19-15651573-C-G

gnomAD v4: 19-15540762-C-G

MyVariant Identifiers: chr19:g.15651573C>G (hg19) chr19:g.15540762C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540762C>G , CM000681.2:g.15540762C>G	GRCh38
NC_000019.9:g.15651573C>G , CM000681.1:g.15651573C>G	GRCh37
NC_000019.8:g.15512573C>G	NCBI36
NG_007987.1:g.37238C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+45C>G MANE Select	ENSP00000269703.1:n.939+45C>G
ENST00000269703.7:c.939+45C>G	ENSP00000269703.1:n.939+45C>G
ENST00000601005.2:c.939+45C>G	ENSP00000469866.1:n.939+45C>G
NM_173483.3:c.939+45C>G	NP_775754.2:n.939+45C>G
XM_011527692.1:c.939+45C>G	XP_011525994.1:n.939+45C>G
XM_011527693.1:c.939+45C>G	XP_011525995.1:n.939+45C>G
XM_011527692.2:c.939+45C>G	XP_011525994.1:n.939+45C>G
XM_011527693.2:c.939+45C>G	XP_011525995.1:n.939+45C>G
NM_173483.4:c.939+45C>G MANE Select	NP_775754.2:n.939+45C>G