Canonical Allele Identifier: CA632130233
Gene: CYP4F2 HGNC NCBI

Linked Data

dbSNP Id: rs1458064172
gnomAD v2: 19-15990338-G-T
gnomAD v3: 19-15879528-G-T
gnomAD v4: 19-15879528-G-T
MyVariant Identifiers: chr19:g.15990338G>T (hg19) chr19:g.15879528G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879528G>T , CM000681.2:g.15879528G>T GRCh38
NC_000019.9:g.15990338G>T , CM000681.1:g.15990338G>T GRCh37
NC_000019.8:g.15851338G>T NCBI36
NG_007971.2:g.23547C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.1314+76C>A MANE Select ENSP00000221700.3:n.1314+76C>A
ENST00000011989.11:c.1314+76C>A ENSP00000011989.8:n.1314+76C>A
ENST00000221700.10:c.1314+76C>A ENSP00000221700.3:n.1314+76C>A
ENST00000392846.7:n.1257+76C>A
ENST00000589654.2:c.103-100C>A
NM_001082.4:c.1314+76C>A NP_001073.3:n.1314+76C>A
NM_001082.5:c.1314+76C>A MANE Select NP_001073.3:n.1314+76C>A
Search 100 bp 5'
Search 100 bp 3'