Canonical Allele Identifier: CA305910153
Gene: CYP4F2 HGNC NCBI

Linked Data

dbSNP Id: rs967317071
gnomAD v3: 19-15897784-C-T
gnomAD v4: 19-15897784-C-T
MyVariant Identifiers: chr19:g.16008594C>T (hg19) chr19:g.15897784C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897784C>T , CM000681.2:g.15897784C>T GRCh38
NC_000019.9:g.16008594C>T , CM000681.1:g.16008594C>T GRCh37
NC_000019.8:g.15869594C>T NCBI36
NG_007971.2:g.5291G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.-1-172G>A MANE Select ENSP00000221700.3:n.-1-172G>A
ENST00000011989.11:c.-1-172G>A ENSP00000011989.8:n.-1-172G>A
ENST00000221700.10:c.-1-172G>A ENSP00000221700.3:n.-1-172G>A
ENST00000392846.7:n.49+242G>A
ENST00000587671.2:c.-1-172G>A ENSP00000467443.2:n.-1-172G>A
ENST00000608168.1:n.53-172G>A
NM_001082.4:c.-1-172G>A NP_001073.3:n.-1-172G>A
NM_001082.5:c.-1-172G>A MANE Select NP_001073.3:n.-1-172G>A
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