Canonical Allele Identifier: CA2336317177

Gene: CYP2F1

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41128246G>T , CM000681.2:g.41128246G>T	GRCh38
NC_000019.9:g.41634151G>T , CM000681.1:g.41634151G>T	GRCh37
NC_000019.8:g.46325991G>T	NCBI36
NG_007930.1:g.18799G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331105.7:c.*164G>T MANE Select	ENSP00000333534.2:n.*164G>T
ENST00000331105.6:c.*164G>T	ENSP00000333534.2:n.*164G>T
ENST00000439903.2:c.590G>T
ENST00000532164.2:c.*619G>T	ENSP00000471416.1:n.*619G>T
NM_000774.3:c.*164G>T	NP_000765.2:n.*164G>T
XM_011526553.1:c.*164G>T	XP_011524855.1:n.*164G>T
XM_011526555.1:c.*229G>T	XP_011524857.1:n.*229G>T
XR_935756.1:n.1794G>T
NM_000774.4:c.*164G>T	NP_000765.2:n.*164G>T
NR_135528.1:n.1654G>T
XM_011526553.2:c.*164G>T	XP_011524855.1:n.*164G>T
XM_011526555.3:c.*229G>T	XP_011524857.1:n.*229G>T
XM_017026385.1:c.*164G>T	XP_016881874.1:n.*164G>T
NM_000774.5:c.*164G>T MANE Select	NP_000765.2:n.*164G>T
NR_135528.2:n.1654G>T