Canonical Allele Identifier: CA1707951

Gene: CYP26B1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.72134831A>G , CM000664.2:g.72134831A>G	GRCh38
NC_000002.11:g.72361960A>G , CM000664.1:g.72361960A>G	GRCh37
NC_000002.10:g.72215468A>G	NCBI36
NG_007957.1:g.18004T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_019885.4:c.791T>C MANE Select	NP_063938.1:p.Leu264Ser
ENST00000001146.7:c.791T>C MANE Select	ENSP00000001146.2:p.Leu264Ser
NM_001277742.1:c.566T>C	NP_001264671.1:p.Leu189Ser
NM_001277742.2:c.566T>C	NP_001264671.1:p.Leu189Ser
NM_019885.3:c.791T>C	NP_063938.1:p.Leu264Ser
ENST00000001146.6:c.791T>C	ENSP00000001146.2:p.Leu264Ser
ENST00000412253.1:c.218T>C	ENSP00000401465.1:p.Leu73Ser
ENST00000546307.5:c.566T>C	ENSP00000443304.1:p.Leu189Ser
XM_005264433.3:c.617T>C	XP_005264490.1:p.Leu206Ser
XM_005264433.4:c.617T>C	XP_005264490.1:p.Leu206Ser
XM_011532988.1:c.218T>C	XP_011531290.1:p.Leu73Ser