Canonical Allele Identifier: CA9274138
Gene: CYP4F2 HGNC NCBI

Linked Data

dbSNP Id: rs758896400
ExAC: 19:16008248 G / A
gnomAD v2: 19-16008248-G-A
gnomAD v4: 19-15897438-G-A
MyVariant Identifiers: chr19:g.16008248G>A (hg19) chr19:g.15897438G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897438G>A , CM000681.2:g.15897438G>A GRCh38
NC_000019.9:g.16008248G>A , CM000681.1:g.16008248G>A GRCh37
NC_000019.8:g.15869248G>A NCBI36
NG_007971.2:g.5637C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.174C>T MANE Select ENSP00000221700.3:p.Asn58=
ENST00000011989.11:c.174C>T ENSP00000011989.8:p.Asn58=
ENST00000221700.10:c.174C>T ENSP00000221700.3:p.Asn58=
ENST00000392846.7:n.49+588C>T
ENST00000586927.2:c.174C>T ENSP00000465514.1:p.Asn58=
ENST00000587671.2:c.174C>T ENSP00000467443.2:p.Asn58=
ENST00000608168.1:n.227C>T
NM_001082.4:c.174C>T NP_001073.3:p.Asn58=
NM_001082.5:c.174C>T MANE Select NP_001073.3:p.Asn58=
Search 100 bp 5'
Search 100 bp 3'