Canonical Allele Identifier: CA9269751
Gene: CYP4F22 HGNC NCBI

Linked Data

dbSNP Id: rs62113200
ExAC: 19:15651549 A / G
gnomAD v2: 19-15651549-A-G
gnomAD v3: 19-15540738-A-G
gnomAD v4: 19-15540738-A-G
MyVariant Identifiers: chr19:g.15651549A>G (hg19) chr19:g.15651549_15651550delinsGT (hg19) chr19:g.15651549_15651551delinsGTT (hg19) chr19:g.15540738A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540738A>G , CM000681.2:g.15540738A>G GRCh38
NC_000019.9:g.15651549A>G , CM000681.1:g.15651549A>G GRCh37
NC_000019.8:g.15512549A>G NCBI36
NG_007987.1:g.37214A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.939+21A>G MANE Select ENSP00000269703.1:n.939+21A>G
ENST00000269703.7:c.939+21A>G ENSP00000269703.1:n.939+21A>G
ENST00000601005.2:c.939+21A>G ENSP00000469866.1:n.939+21A>G
NM_173483.3:c.939+21A>G NP_775754.2:n.939+21A>G
XM_011527692.1:c.939+21A>G XP_011525994.1:n.939+21A>G
XM_011527693.1:c.939+21A>G XP_011525995.1:n.939+21A>G
XM_011527692.2:c.939+21A>G XP_011525994.1:n.939+21A>G
XM_011527693.2:c.939+21A>G XP_011525995.1:n.939+21A>G
NM_173483.4:c.939+21A>G MANE Select NP_775754.2:n.939+21A>G
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