Canonical Allele Identifier: CA2325101798
Gene: CYP4F2 HGNC NCBI

Linked Data

dbSNP Id: rs3093158
gnomAD v4: 19-15889356-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15889356C>A , CM000681.2:g.15889356C>A GRCh38
NC_000019.9:g.16000166C>A , CM000681.1:g.16000166C>A GRCh37
NC_000019.8:g.15861166C>A NCBI36
NG_007971.2:g.13719G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000221700.11:c.918+67G>T MANE Select ENSP00000221700.3:n.918+67G>T
ENST00000011989.11:c.918+67G>T ENSP00000011989.8:n.918+67G>T
ENST00000221700.10:c.918+67G>T ENSP00000221700.3:n.918+67G>T
ENST00000392846.7:n.861+67G>T
ENST00000587671.2:c.*503+67G>T ENSP00000467443.2:n.*503+67G>T
NM_001082.4:c.918+67G>T NP_001073.3:n.918+67G>T
NM_001082.5:c.918+67G>T MANE Select NP_001073.3:n.918+67G>T
Search 100 bp 5'
Search 100 bp 3'