Canonical Allele Identifier: CA404579712
Gene: CYP4F2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.16008233G>C (hg19) chr19:g.15897423G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897423G>C , CM000681.2:g.15897423G>C GRCh38
NC_000019.9:g.16008233G>C , CM000681.1:g.16008233G>C GRCh37
NC_000019.8:g.15869233G>C NCBI36
NG_007971.2:g.5652C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.189C>G MANE Select ENSP00000221700.3:p.His63Gln
ENST00000011989.11:c.189C>G ENSP00000011989.8:p.His63Gln
ENST00000221700.10:c.189C>G ENSP00000221700.3:p.His63Gln
ENST00000392846.7:n.49+603C>G
ENST00000586927.2:c.189C>G ENSP00000465514.1:p.His63Gln
ENST00000587671.2:c.189C>G ENSP00000467443.2:p.His63Gln
ENST00000608168.1:n.242C>G
NM_001082.4:c.189C>G NP_001073.3:p.His63Gln
NM_001082.5:c.189C>G MANE Select NP_001073.3:p.His63Gln
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