Canonical Allele Identifier: CA9269763
Gene: CYP4F22 HGNC NCBI

Linked Data

dbSNP Id: rs756529201
ExAC: 19:15651559 TC / T
gnomAD v2: 19-15651559-TC-T
gnomAD v4: 19-15540748-TC-T
MyVariant Identifiers: chr19:g.15651560del (hg19) chr19:g.15651562_15651564delinsGA (hg19) chr19:g.15651562_15651565delinsGAG (hg19) chr19:g.15540749del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540751del , CM000681.2:g.15540751del GRCh38
NC_000019.9:g.15651562del , CM000681.1:g.15651562del GRCh37
NC_000019.8:g.15512562del NCBI36
NG_007987.1:g.37227del

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.939+34del MANE Select ENSP00000269703.1:n.939+34del
ENST00000269703.7:c.939+34del ENSP00000269703.1:n.939+34del
ENST00000601005.2:c.939+34del ENSP00000469866.1:n.939+34del
NM_173483.3:c.939+34del NP_775754.2:n.939+34del
XM_011527692.1:c.939+34del XP_011525994.1:n.939+34del
XM_011527693.1:c.939+34del XP_011525995.1:n.939+34del
XM_011527692.2:c.939+34del XP_011525994.1:n.939+34del
XM_011527693.2:c.939+34del XP_011525995.1:n.939+34del
NM_173483.4:c.939+34del MANE Select NP_775754.2:n.939+34del
Search 100 bp 5'
Search 100 bp 3'