Canonical Allele Identifier: CA632130189
Gene: CYP4F2 HGNC NCBI

Linked Data

dbSNP Id: rs1235015338
gnomAD v2: 19-16000151-T-A
gnomAD v3: 19-15889341-T-A
gnomAD v4: 19-15889341-T-A
MyVariant Identifiers: chr19:g.16000151T>A (hg19) chr19:g.15889341T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15889341T>A , CM000681.2:g.15889341T>A GRCh38
NC_000019.9:g.16000151T>A , CM000681.1:g.16000151T>A GRCh37
NC_000019.8:g.15861151T>A NCBI36
NG_007971.2:g.13734A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.918+82A>T MANE Select ENSP00000221700.3:n.918+82A>T
ENST00000011989.11:c.918+82A>T ENSP00000011989.8:n.918+82A>T
ENST00000221700.10:c.918+82A>T ENSP00000221700.3:n.918+82A>T
ENST00000392846.7:n.861+82A>T
ENST00000587671.2:c.*503+82A>T ENSP00000467443.2:n.*503+82A>T
NM_001082.4:c.918+82A>T NP_001073.3:n.918+82A>T
NM_001082.5:c.918+82A>T MANE Select NP_001073.3:n.918+82A>T
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