Canonical Allele Identifier: CA9273662
Gene: CYP4F2 HGNC NCBI

Linked Data

dbSNP Id: rs752124224
ExAC: 19:15990268 G / T
gnomAD v2: 19-15990268-G-T
gnomAD v4: 19-15879458-G-T
MyVariant Identifiers: chr19:g.15990268G>T (hg19) chr19:g.15879458G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879458G>T , CM000681.2:g.15879458G>T GRCh38
NC_000019.9:g.15990268G>T , CM000681.1:g.15990268G>T GRCh37
NC_000019.8:g.15851268G>T NCBI36
NG_007971.2:g.23617C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.1315-30C>A MANE Select ENSP00000221700.3:n.1315-30C>A
ENST00000011989.11:c.1315-30C>A ENSP00000011989.8:n.1315-30C>A
ENST00000221700.10:c.1315-30C>A ENSP00000221700.3:n.1315-30C>A
ENST00000392846.7:n.1258-30C>A
ENST00000589654.2:c.103-30C>A
NM_001082.4:c.1315-30C>A NP_001073.3:n.1315-30C>A
NM_001082.5:c.1315-30C>A MANE Select NP_001073.3:n.1315-30C>A
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