Canonical Allele Identifier: CA2583145778
Gene: CYP4F2 HGNC NCBI

Linked Data

gnomAD v4: 19-15889329-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15889329C>G , CM000681.2:g.15889329C>G GRCh38
NC_000019.9:g.16000139C>G , CM000681.1:g.16000139C>G GRCh37
NC_000019.8:g.15861139C>G NCBI36
NG_007971.2:g.13746G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.918+94G>C MANE Select ENSP00000221700.3:n.918+94G>C
ENST00000011989.11:c.918+94G>C ENSP00000011989.8:n.918+94G>C
ENST00000221700.10:c.918+94G>C ENSP00000221700.3:n.918+94G>C
ENST00000392846.7:n.861+94G>C
ENST00000587671.2:c.*503+94G>C ENSP00000467443.2:n.*503+94G>C
NM_001082.4:c.918+94G>C NP_001073.3:n.918+94G>C
NM_001082.5:c.918+94G>C MANE Select NP_001073.3:n.918+94G>C
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