Canonical Allele Identifier: CA305909222
Gene: CYP4F2 HGNC NCBI

Linked Data

dbSNP Id: rs190172586
gnomAD v3: 19-15897143-C-T
gnomAD v4: 19-15897143-C-T
MyVariant Identifiers: chr19:g.16007953C>T (hg19) chr19:g.15897143C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897143C>T , CM000681.2:g.15897143C>T GRCh38
NC_000019.9:g.16007953C>T , CM000681.1:g.16007953C>T GRCh37
NC_000019.8:g.15868953C>T NCBI36
NG_007971.2:g.5932G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.198+271G>A MANE Select ENSP00000221700.3:n.198+271G>A
ENST00000011989.11:c.198+271G>A ENSP00000011989.8:n.198+271G>A
ENST00000221700.10:c.198+271G>A ENSP00000221700.3:n.198+271G>A
ENST00000392846.7:n.49+883G>A
ENST00000586927.2:c.198+271G>A ENSP00000465514.1:n.198+271G>A
ENST00000587671.2:c.198+271G>A ENSP00000467443.2:n.198+271G>A
ENST00000608168.1:n.251+271G>A
NM_001082.4:c.198+271G>A NP_001073.3:n.198+271G>A
NM_001082.5:c.198+271G>A MANE Select NP_001073.3:n.198+271G>A
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