Canonical Allele Identifier: CA305909194
Gene: CYP4F2 HGNC NCBI

Linked Data

dbSNP Id: rs1054033347
gnomAD v3: 19-15897138-A-G
gnomAD v4: 19-15897138-A-G
MyVariant Identifiers: chr19:g.16007948A>G (hg19) chr19:g.15897138A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897138A>G , CM000681.2:g.15897138A>G GRCh38
NC_000019.9:g.16007948A>G , CM000681.1:g.16007948A>G GRCh37
NC_000019.8:g.15868948A>G NCBI36
NG_007971.2:g.5937T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.198+276T>C MANE Select ENSP00000221700.3:n.198+276T>C
ENST00000011989.11:c.198+276T>C ENSP00000011989.8:n.198+276T>C
ENST00000221700.10:c.198+276T>C ENSP00000221700.3:n.198+276T>C
ENST00000392846.7:n.49+888T>C
ENST00000586927.2:c.198+276T>C ENSP00000465514.1:n.198+276T>C
ENST00000587671.2:c.198+276T>C ENSP00000467443.2:n.198+276T>C
ENST00000608168.1:n.251+276T>C
NM_001082.4:c.198+276T>C NP_001073.3:n.198+276T>C
NM_001082.5:c.198+276T>C MANE Select NP_001073.3:n.198+276T>C
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