Canonical Allele Identifier: CA631973770
Gene: CYP4F2 HGNC NCBI

Linked Data

dbSNP Id: rs1421084850
gnomAD v2: 19-15990279-C-A
gnomAD v4: 19-15879469-C-A
MyVariant Identifiers: chr19:g.15990279C>A (hg19) chr19:g.15879469C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879469C>A , CM000681.2:g.15879469C>A GRCh38
NC_000019.9:g.15990279C>A , CM000681.1:g.15990279C>A GRCh37
NC_000019.8:g.15851279C>A NCBI36
NG_007971.2:g.23606G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.1315-41G>T MANE Select ENSP00000221700.3:n.1315-41G>T
ENST00000011989.11:c.1315-41G>T ENSP00000011989.8:n.1315-41G>T
ENST00000221700.10:c.1315-41G>T ENSP00000221700.3:n.1315-41G>T
ENST00000392846.7:n.1258-41G>T
ENST00000589654.2:c.103-41G>T
NM_001082.4:c.1315-41G>T NP_001073.3:n.1315-41G>T
NM_001082.5:c.1315-41G>T MANE Select NP_001073.3:n.1315-41G>T
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