Canonical Allele Identifier: CA783707481
Gene: CYP4F2 HGNC NCBI

Linked Data

dbSNP Id: rs1358865684
MyVariant Identifiers: chr19:g.15990243A>C (hg19) chr19:g.15879433A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879433A>C , CM000681.2:g.15879433A>C GRCh38
NC_000019.9:g.15990243A>C , CM000681.1:g.15990243A>C GRCh37
NC_000019.8:g.15851243A>C NCBI36
NG_007971.2:g.23642T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000221700.11:c.1315-5T>G MANE Select ENSP00000221700.3:n.1315-5T>G
ENST00000011989.11:c.1315-5T>G ENSP00000011989.8:n.1315-5T>G
ENST00000221700.10:c.1315-5T>G ENSP00000221700.3:n.1315-5T>G
ENST00000392846.7:n.1258-5T>G
ENST00000589654.2:c.103-5T>G
NM_001082.4:c.1315-5T>G NP_001073.3:n.1315-5T>G
NM_001082.5:c.1315-5T>G MANE Select NP_001073.3:n.1315-5T>G
Search 100 bp 5'
Search 100 bp 3'