Canonical Allele Identifier: CA9273660
Gene: CYP4F2 HGNC NCBI

Linked Data

dbSNP Id: rs376173329
ExAC: 19:15990264 T / C
gnomAD v2: 19-15990264-T-C
gnomAD v3: 19-15879454-T-C
gnomAD v4: 19-15879454-T-C
MyVariant Identifiers: chr19:g.15990264T>C (hg19) chr19:g.15879454T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879454T>C , CM000681.2:g.15879454T>C GRCh38
NC_000019.9:g.15990264T>C , CM000681.1:g.15990264T>C GRCh37
NC_000019.8:g.15851264T>C NCBI36
NG_007971.2:g.23621A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000221700.11:c.1315-26A>G MANE Select ENSP00000221700.3:n.1315-26A>G
ENST00000011989.11:c.1315-26A>G ENSP00000011989.8:n.1315-26A>G
ENST00000221700.10:c.1315-26A>G ENSP00000221700.3:n.1315-26A>G
ENST00000392846.7:n.1258-26A>G
ENST00000589654.2:c.103-26A>G
NM_001082.4:c.1315-26A>G NP_001073.3:n.1315-26A>G
NM_001082.5:c.1315-26A>G MANE Select NP_001073.3:n.1315-26A>G
Search 100 bp 5'
Search 100 bp 3'