Canonical Allele Identifier: CA2325105733
Gene: CYP4F2 HGNC NCBI

Linked Data

dbSNP Id: rs2978637

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897782A>C , CM000681.2:g.15897782A>C GRCh38
NC_000019.9:g.16008592A>C , CM000681.1:g.16008592A>C GRCh37
NC_000019.8:g.15869592A>C NCBI36
NG_007971.2:g.5293T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.-1-170T>G MANE Select ENSP00000221700.3:n.-1-170T>G
ENST00000011989.11:c.-1-170T>G ENSP00000011989.8:n.-1-170T>G
ENST00000221700.10:c.-1-170T>G ENSP00000221700.3:n.-1-170T>G
ENST00000392846.7:n.49+244T>G
ENST00000587671.2:c.-1-170T>G ENSP00000467443.2:n.-1-170T>G
ENST00000608168.1:n.53-170T>G
NM_001082.4:c.-1-170T>G NP_001073.3:n.-1-170T>G
NM_001082.5:c.-1-170T>G MANE Select NP_001073.3:n.-1-170T>G