Canonical Allele Identifier: CA404572532
Gene: CYP4F2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879356C>A , CM000681.2:g.15879356C>A GRCh38
NC_000019.9:g.15990166C>A , CM000681.1:g.15990166C>A GRCh37
NC_000019.8:g.15851166C>A NCBI36
NG_007971.2:g.23719G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.1387G>T MANE Select ENSP00000221700.3:p.Ala463Ser
ENST00000011989.11:c.1387G>T ENSP00000011989.8:p.Ala463Ser
ENST00000221700.10:c.1387G>T ENSP00000221700.3:p.Ala463Ser
ENST00000392846.7:n.1330G>T
ENST00000589654.2:c.175G>T
NM_001082.4:c.1387G>T NP_001073.3:p.Ala463Ser
NM_001082.5:c.1387G>T MANE Select NP_001073.3:p.Ala463Ser