Canonical Allele Identifier: CA2583145451
Gene: CYP4F2 HGNC NCBI

Linked Data

gnomAD v4: 19-15879458-G-C
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Genomic Alleles

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

Transcript Alleles

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