Canonical Allele Identifier: CA783646422
Gene: CYP4F22 HGNC NCBI

Linked Data

dbSNP Id: rs372614865
MyVariant Identifiers: chr19:g.15651551T>C (hg19) chr19:g.15540740T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540740T>C , CM000681.2:g.15540740T>C GRCh38
NC_000019.9:g.15651551T>C , CM000681.1:g.15651551T>C GRCh37
NC_000019.8:g.15512551T>C NCBI36
NG_007987.1:g.37216T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.939+23T>C MANE Select ENSP00000269703.1:n.939+23T>C
ENST00000269703.7:c.939+23T>C ENSP00000269703.1:n.939+23T>C
ENST00000601005.2:c.939+23T>C ENSP00000469866.1:n.939+23T>C
NM_173483.3:c.939+23T>C NP_775754.2:n.939+23T>C
XM_011527692.1:c.939+23T>C XP_011525994.1:n.939+23T>C
XM_011527693.1:c.939+23T>C XP_011525995.1:n.939+23T>C
XM_011527692.2:c.939+23T>C XP_011525994.1:n.939+23T>C
XM_011527693.2:c.939+23T>C XP_011525995.1:n.939+23T>C
NM_173483.4:c.939+23T>C MANE Select NP_775754.2:n.939+23T>C
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