Canonical Allele Identifier: CA16043077
Gene: CYP4F22 HGNC NCBI

Linked Data

ClinVar Variation Id: 372938
ClinVar RCV Id: RCV000414461
dbSNP Id: rs1057518087
MyVariant Identifiers: chr19:g.15640510C>G (hg19) chr19:g.15529699C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15529699C>G , CM000681.2:g.15529699C>G GRCh38
NC_000019.9:g.15640510C>G , CM000681.1:g.15640510C>G GRCh37
NC_000019.8:g.15501510C>G NCBI36
NG_007987.1:g.26175C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000269703.8:c.223-10C>G MANE Select ENSP00000269703.1:n.223-10C>G
ENST00000269703.7:c.223-10C>G ENSP00000269703.1:n.223-10C>G
ENST00000601005.2:c.223-10C>G ENSP00000469866.1:n.223-10C>G
NM_173483.3:c.223-10C>G NP_775754.2:n.223-10C>G
XM_011527692.1:c.223-10C>G XP_011525994.1:n.223-10C>G
XM_011527693.1:c.223-10C>G XP_011525995.1:n.223-10C>G
XM_011527692.2:c.223-10C>G XP_011525994.1:n.223-10C>G
XM_011527693.2:c.223-10C>G XP_011525995.1:n.223-10C>G
NM_173483.4:c.223-10C>G MANE Select NP_775754.2:n.223-10C>G
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