Canonical Allele Identifier: CA2583107946
Gene: CYP4F22 HGNC NCBI

Linked Data

gnomAD v4: 19-15540345-C-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540345C>G , CM000681.2:g.15540345C>G GRCh38
NC_000019.9:g.15651156C>G , CM000681.1:g.15651156C>G GRCh37
NC_000019.8:g.15512156C>G NCBI36
NG_007987.1:g.36821C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.672-105C>G MANE Select ENSP00000269703.1:n.672-105C>G
ENST00000269703.7:c.672-105C>G ENSP00000269703.1:n.672-105C>G
ENST00000601005.2:c.672-105C>G ENSP00000469866.1:n.672-105C>G
NM_173483.3:c.672-105C>G NP_775754.2:n.672-105C>G
XM_011527692.1:c.672-105C>G XP_011525994.1:n.672-105C>G
XM_011527693.1:c.672-105C>G XP_011525995.1:n.672-105C>G
XM_011527692.2:c.672-105C>G XP_011525994.1:n.672-105C>G
XM_011527693.2:c.672-105C>G XP_011525995.1:n.672-105C>G
NM_173483.4:c.672-105C>G MANE Select NP_775754.2:n.672-105C>G
Search 100 bp 5'
Search 100 bp 3'