Canonical Allele Identifier: CA783707156
Gene: CYP4F2 HGNC NCBI

Linked Data

dbSNP Id: rs1167504018
gnomAD v3: 19-15879186-C-A
gnomAD v4: 19-15879186-C-A
MyVariant Identifiers: chr19:g.15989996C>A (hg19) chr19:g.15879186C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879186C>A , CM000681.2:g.15879186C>A GRCh38
NC_000019.9:g.15989996C>A , CM000681.1:g.15989996C>A GRCh37
NC_000019.8:g.15850996C>A NCBI36
NG_007971.2:g.23889G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.1397+160G>T MANE Select ENSP00000221700.3:n.1397+160G>T
ENST00000011989.11:c.1397+160G>T ENSP00000011989.8:n.1397+160G>T
ENST00000221700.10:c.1397+160G>T ENSP00000221700.3:n.1397+160G>T
ENST00000392846.7:n.1340+160G>T
ENST00000589654.2:c.185+160G>T
NM_001082.4:c.1397+160G>T NP_001073.3:n.1397+160G>T
NM_001082.5:c.1397+160G>T MANE Select NP_001073.3:n.1397+160G>T
Search 100 bp 5'
Search 100 bp 3'