Canonical Allele Identifier: CA2576658989

Gene: CYP4F2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15879285G>C , CM000681.2:g.15879285G>C	GRCh38
NC_000019.9:g.15990095G>C , CM000681.1:g.15990095G>C	GRCh37
NC_000019.8:g.15851095G>C	NCBI36
NG_007971.2:g.23790C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.1397+61C>G MANE Select	ENSP00000221700.3:n.1397+61C>G
ENST00000011989.11:c.1397+61C>G	ENSP00000011989.8:n.1397+61C>G
ENST00000221700.10:c.1397+61C>G	ENSP00000221700.3:n.1397+61C>G
ENST00000392846.7:n.1340+61C>G
ENST00000589654.2:c.185+61C>G
NM_001082.4:c.1397+61C>G	NP_001073.3:n.1397+61C>G
NM_001082.5:c.1397+61C>G MANE Select	NP_001073.3:n.1397+61C>G