Canonical Allele Identifier: CA783707175
Gene: CYP4F2 HGNC NCBI

Linked Data

dbSNP Id: rs1250833530
gnomAD v3: 19-15879212-T-C
gnomAD v4: 19-15879212-T-C
MyVariant Identifiers: chr19:g.15990022T>C (hg19) chr19:g.15879212T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879212T>C , CM000681.2:g.15879212T>C GRCh38
NC_000019.9:g.15990022T>C , CM000681.1:g.15990022T>C GRCh37
NC_000019.8:g.15851022T>C NCBI36
NG_007971.2:g.23863A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.1397+134A>G MANE Select ENSP00000221700.3:n.1397+134A>G
ENST00000011989.11:c.1397+134A>G ENSP00000011989.8:n.1397+134A>G
ENST00000221700.10:c.1397+134A>G ENSP00000221700.3:n.1397+134A>G
ENST00000392846.7:n.1340+134A>G
ENST00000589654.2:c.185+134A>G
NM_001082.4:c.1397+134A>G NP_001073.3:n.1397+134A>G
NM_001082.5:c.1397+134A>G MANE Select NP_001073.3:n.1397+134A>G
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