Canonical Allele Identifier: CA2642410966
Gene: CYP4F22 HGNC NCBI

Linked Data

gnomAD v4: 19-15529630-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15529630A>G , CM000681.2:g.15529630A>G GRCh38
NC_000019.9:g.15640441A>G , CM000681.1:g.15640441A>G GRCh37
NC_000019.8:g.15501441A>G NCBI36
NG_007987.1:g.26106A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000269703.8:c.223-79A>G MANE Select ENSP00000269703.1:n.223-79A>G
ENST00000269703.7:c.223-79A>G ENSP00000269703.1:n.223-79A>G
ENST00000601005.2:c.223-79A>G ENSP00000469866.1:n.223-79A>G
NM_173483.3:c.223-79A>G NP_775754.2:n.223-79A>G
XM_011527692.1:c.223-79A>G XP_011525994.1:n.223-79A>G
XM_011527693.1:c.223-79A>G XP_011525995.1:n.223-79A>G
XM_011527692.2:c.223-79A>G XP_011525994.1:n.223-79A>G
XM_011527693.2:c.223-79A>G XP_011525995.1:n.223-79A>G
NM_173483.4:c.223-79A>G MANE Select NP_775754.2:n.223-79A>G
Search 100 bp 5'
Search 100 bp 3'