Canonical Allele Identifier: CA2838371662

Gene: HMBS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119084935T>C , CM000673.2:g.119084935T>C	GRCh38
NC_000011.9:g.118955645T>C , CM000673.1:g.118955645T>C	GRCh37
NC_000011.8:g.118460855T>C	NCBI36
NG_008093.1:g.5059T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442944.7:c.-99T>C	ENSP00000392041.3:n.-99T>C
ENST00000536813.6:c.-233T>C	ENSP00000438726.2:n.-233T>C
ENST00000546302.6:c.-99T>C	ENSP00000445599.1:n.-99T>C
ENST00000640813.1:c.-150T>C	ENSP00000491061.1:n.-150T>C
ENST00000652429.1:c.-99T>C MANE Select	ENSP00000498786.1:n.-99T>C
ENST00000278715.7:c.-99T>C	ENSP00000278715.3:n.-99T>C
ENST00000442944.6:c.-233T>C	ENSP00000392041.2:n.-233T>C
ENST00000535793.5:c.-99T>C	ENSP00000439904.1:n.-99T>C
ENST00000536185.5:n.70T>C
ENST00000536813.5:c.-99T>C	ENSP00000438726.1:n.-99T>C
ENST00000537841.5:c.-241T>C	ENSP00000444730.1:n.-241T>C
ENST00000542044.5:n.27T>C
ENST00000542729.5:c.-241T>C	ENSP00000443058.1:n.-241T>C
ENST00000542822.5:c.-99T>C	ENSP00000444817.1:n.-99T>C
ENST00000543090.5:c.-99T>C	ENSP00000445429.1:n.-99T>C
ENST00000543821.5:n.48T>C
ENST00000544387.5:c.-99T>C	ENSP00000438424.1:n.-99T>C
ENST00000545621.5:c.-99T>C	ENSP00000444849.1:n.-99T>C
ENST00000545901.5:n.55T>C
ENST00000546302.5:c.-99T>C	ENSP00000445599.1:n.-99T>C
NM_000190.3:c.-99T>C	NP_000181.2:n.-99T>C
NM_001258208.1:c.-99T>C	NP_001245137.1:n.-99T>C
NM_001258209.1:c.-241T>C	NP_001245138.1:n.-241T>C
XM_005271531.1:c.-241T>C	XP_005271588.1:n.-241T>C
XM_005271532.1:c.-217T>C	XP_005271589.1:n.-217T>C
XM_005271533.2:c.-99T>C	XP_005271590.1:n.-99T>C
NM_000190.4:c.-99T>C MANE Select	NP_000181.2:n.-99T>C
XM_005271533.3:c.-99T>C	XP_005271590.1:n.-99T>C
XM_024448460.1:c.-99T>C	XP_024304228.1:n.-99T>C
NM_001258208.2:c.-99T>C	NP_001245137.1:n.-99T>C
NM_001258209.2:c.-241T>C	NP_001245138.1:n.-241T>C