Canonical Allele Identifier: CA9274155
Gene: CYP4F2 HGNC NCBI

Linked Data

dbSNP Id: rs201106180
ExAC: 19:16008304 C / T
gnomAD v2: 19-16008304-C-T
gnomAD v3: 19-15897494-C-T
gnomAD v4: 19-15897494-C-T
MyVariant Identifiers: chr19:g.16008304C>T (hg19) chr19:g.15897494C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897494C>T , CM000681.2:g.15897494C>T GRCh38
NC_000019.9:g.16008304C>T , CM000681.1:g.16008304C>T GRCh37
NC_000019.8:g.15869304C>T NCBI36
NG_007971.2:g.5581G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000221700.11:c.118G>A MANE Select ENSP00000221700.3:p.Ala40Thr
ENST00000011989.11:c.118G>A ENSP00000011989.8:p.Ala40Thr
ENST00000221700.10:c.118G>A ENSP00000221700.3:p.Ala40Thr
ENST00000392846.7:n.49+532G>A
ENST00000586927.2:c.118G>A ENSP00000465514.1:p.Ala40Thr
ENST00000587671.2:c.118G>A ENSP00000467443.2:p.Ala40Thr
ENST00000608168.1:n.171G>A
NM_001082.4:c.118G>A NP_001073.3:p.Ala40Thr
NM_001082.5:c.118G>A MANE Select NP_001073.3:p.Ala40Thr
Search 100 bp 5'
Search 100 bp 3'