Canonical Allele Identifier: CA305879661
Gene: CYP4F2 HGNC NCBI

Linked Data

dbSNP Id: rs971228914
gnomAD v4: 19-15879211-C-T
MyVariant Identifiers: chr19:g.15990021C>T (hg19) chr19:g.15879211C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879211C>T , CM000681.2:g.15879211C>T GRCh38
NC_000019.9:g.15990021C>T , CM000681.1:g.15990021C>T GRCh37
NC_000019.8:g.15851021C>T NCBI36
NG_007971.2:g.23864G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.1397+135G>A MANE Select ENSP00000221700.3:n.1397+135G>A
ENST00000011989.11:c.1397+135G>A ENSP00000011989.8:n.1397+135G>A
ENST00000221700.10:c.1397+135G>A ENSP00000221700.3:n.1397+135G>A
ENST00000392846.7:n.1340+135G>A
ENST00000589654.2:c.185+135G>A
NM_001082.4:c.1397+135G>A NP_001073.3:n.1397+135G>A
NM_001082.5:c.1397+135G>A MANE Select NP_001073.3:n.1397+135G>A
Search 100 bp 5'
Search 100 bp 3'