Canonical Allele Identifier: CA2616352474

Gene: HMBS

Linked Data

• gnomAD v4: 11-119084925-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119084925C>A , CM000673.2:g.119084925C>A	GRCh38
NC_000011.9:g.118955635C>A , CM000673.1:g.118955635C>A	GRCh37
NC_000011.8:g.118460845C>A	NCBI36
NG_008093.1:g.5049C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442944.7:c.-109C>A	ENSP00000392041.3:n.-109C>A
ENST00000536813.6:c.-243C>A	ENSP00000438726.2:n.-243C>A
ENST00000546302.6:c.-109C>A	ENSP00000445599.1:n.-109C>A
ENST00000640813.1:c.-160C>A	ENSP00000491061.1:n.-160C>A
ENST00000652429.1:c.-109C>A MANE Select	ENSP00000498786.1:n.-109C>A
ENST00000278715.7:c.-109C>A	ENSP00000278715.3:n.-109C>A
ENST00000442944.6:c.-243C>A	ENSP00000392041.2:n.-243C>A
ENST00000535793.5:c.-109C>A	ENSP00000439904.1:n.-109C>A
ENST00000536185.5:n.60C>A
ENST00000536813.5:c.-109C>A	ENSP00000438726.1:n.-109C>A
ENST00000537841.5:c.-251C>A	ENSP00000444730.1:n.-251C>A
ENST00000542044.5:n.17C>A
ENST00000542729.5:c.-251C>A	ENSP00000443058.1:n.-251C>A
ENST00000542822.5:c.-109C>A	ENSP00000444817.1:n.-109C>A
ENST00000543821.5:n.38C>A
ENST00000544387.5:c.-109C>A	ENSP00000438424.1:n.-109C>A
ENST00000545621.5:c.-109C>A	ENSP00000444849.1:n.-109C>A
ENST00000545901.5:n.45C>A
ENST00000546302.5:c.-109C>A	ENSP00000445599.1:n.-109C>A
NM_000190.3:c.-109C>A	NP_000181.2:n.-109C>A
NM_001258208.1:c.-109C>A	NP_001245137.1:n.-109C>A
NM_001258209.1:c.-251C>A	NP_001245138.1:n.-251C>A
XM_005271531.1:c.-251C>A	XP_005271588.1:n.-251C>A
XM_005271532.1:c.-227C>A	XP_005271589.1:n.-227C>A
XM_005271533.2:c.-109C>A	XP_005271590.1:n.-109C>A
NM_000190.4:c.-109C>A MANE Select	NP_000181.2:n.-109C>A
XM_005271533.3:c.-109C>A	XP_005271590.1:n.-109C>A
XM_024448460.1:c.-109C>A	XP_024304228.1:n.-109C>A
NM_001258208.2:c.-109C>A	NP_001245137.1:n.-109C>A
NM_001258209.2:c.-251C>A	NP_001245138.1:n.-251C>A