Canonical Allele Identifier: CA631973750
Gene: CYP4F2 HGNC NCBI

Linked Data

dbSNP Id: rs1180339477
gnomAD v2: 19-15990122-A-C
gnomAD v3: 19-15879312-A-C
gnomAD v4: 19-15879312-A-C
MyVariant Identifiers: chr19:g.15990122A>C (hg19) chr19:g.15879312A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879312A>C , CM000681.2:g.15879312A>C GRCh38
NC_000019.9:g.15990122A>C , CM000681.1:g.15990122A>C GRCh37
NC_000019.8:g.15851122A>C NCBI36
NG_007971.2:g.23763T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.1397+34T>G MANE Select ENSP00000221700.3:n.1397+34T>G
ENST00000011989.11:c.1397+34T>G ENSP00000011989.8:n.1397+34T>G
ENST00000221700.10:c.1397+34T>G ENSP00000221700.3:n.1397+34T>G
ENST00000392846.7:n.1340+34T>G
ENST00000589654.2:c.185+34T>G
NM_001082.4:c.1397+34T>G NP_001073.3:n.1397+34T>G
NM_001082.5:c.1397+34T>G MANE Select NP_001073.3:n.1397+34T>G
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