Canonical Allele Identifier: CA2576658991

Gene: CYP4F2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15879291C>A , CM000681.2:g.15879291C>A	GRCh38
NC_000019.9:g.15990101C>A , CM000681.1:g.15990101C>A	GRCh37
NC_000019.8:g.15851101C>A	NCBI36
NG_007971.2:g.23784G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.1397+55G>T MANE Select	ENSP00000221700.3:n.1397+55G>T
ENST00000011989.11:c.1397+55G>T	ENSP00000011989.8:n.1397+55G>T
ENST00000221700.10:c.1397+55G>T	ENSP00000221700.3:n.1397+55G>T
ENST00000392846.7:n.1340+55G>T
ENST00000589654.2:c.185+55G>T
NM_001082.4:c.1397+55G>T	NP_001073.3:n.1397+55G>T
NM_001082.5:c.1397+55G>T MANE Select	NP_001073.3:n.1397+55G>T