Canonical Allele Identifier: CA305879630
Gene: CYP4F2 HGNC NCBI

Linked Data

dbSNP Id: rs530133717
gnomAD v3: 19-15879150-G-A
gnomAD v4: 19-15879150-G-A
MyVariant Identifiers: chr19:g.15989960G>A (hg19) chr19:g.15879150G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879150G>A , CM000681.2:g.15879150G>A GRCh38
NC_000019.9:g.15989960G>A , CM000681.1:g.15989960G>A GRCh37
NC_000019.8:g.15850960G>A NCBI36
NG_007971.2:g.23925C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.1397+196C>T MANE Select ENSP00000221700.3:n.1397+196C>T
ENST00000011989.11:c.1397+196C>T ENSP00000011989.8:n.1397+196C>T
ENST00000221700.10:c.1397+196C>T ENSP00000221700.3:n.1397+196C>T
ENST00000392846.7:n.1340+196C>T
ENST00000589654.2:c.185+196C>T
NM_001082.4:c.1397+196C>T NP_001073.3:n.1397+196C>T
NM_001082.5:c.1397+196C>T MANE Select NP_001073.3:n.1397+196C>T
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