Canonical Allele Identifier: CA2325096953
Gene: CYP4F2 HGNC NCBI

Linked Data

dbSNP Id: rs1568469259
gnomAD v4: 19-15879444-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879444A>G , CM000681.2:g.15879444A>G GRCh38
NC_000019.9:g.15990254A>G , CM000681.1:g.15990254A>G GRCh37
NC_000019.8:g.15851254A>G NCBI36
NG_007971.2:g.23631T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000221700.11:c.1315-16T>C MANE Select ENSP00000221700.3:n.1315-16T>C
ENST00000011989.11:c.1315-16T>C ENSP00000011989.8:n.1315-16T>C
ENST00000221700.10:c.1315-16T>C ENSP00000221700.3:n.1315-16T>C
ENST00000392846.7:n.1258-16T>C
ENST00000589654.2:c.103-16T>C
NM_001082.4:c.1315-16T>C NP_001073.3:n.1315-16T>C
NM_001082.5:c.1315-16T>C MANE Select NP_001073.3:n.1315-16T>C
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