Canonical Allele Identifier: CA2616352498

Gene: HMBS

Linked Data

• gnomAD v4: 11-119084937-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119084937C>T , CM000673.2:g.119084937C>T	GRCh38
NC_000011.9:g.118955647C>T , CM000673.1:g.118955647C>T	GRCh37
NC_000011.8:g.118460857C>T	NCBI36
NG_008093.1:g.5061C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000442944.7:c.-97C>T	ENSP00000392041.3:n.-97C>T
ENST00000536813.6:c.-231C>T	ENSP00000438726.2:n.-231C>T
ENST00000546302.6:c.-97C>T	ENSP00000445599.1:n.-97C>T
ENST00000640813.1:c.-148C>T	ENSP00000491061.1:n.-148C>T
ENST00000652429.1:c.-97C>T MANE Select	ENSP00000498786.1:n.-97C>T
ENST00000278715.7:c.-97C>T	ENSP00000278715.3:n.-97C>T
ENST00000442944.6:c.-231C>T	ENSP00000392041.2:n.-231C>T
ENST00000535793.5:c.-97C>T	ENSP00000439904.1:n.-97C>T
ENST00000536185.5:n.72C>T
ENST00000536813.5:c.-97C>T	ENSP00000438726.1:n.-97C>T
ENST00000537841.5:c.-239C>T	ENSP00000444730.1:n.-239C>T
ENST00000542044.5:n.29C>T
ENST00000542729.5:c.-239C>T	ENSP00000443058.1:n.-239C>T
ENST00000542822.5:c.-97C>T	ENSP00000444817.1:n.-97C>T
ENST00000543090.5:c.-97C>T	ENSP00000445429.1:n.-97C>T
ENST00000543821.5:n.50C>T
ENST00000544387.5:c.-97C>T	ENSP00000438424.1:n.-97C>T
ENST00000545621.5:c.-97C>T	ENSP00000444849.1:n.-97C>T
ENST00000545901.5:n.57C>T
ENST00000546302.5:c.-97C>T	ENSP00000445599.1:n.-97C>T
NM_000190.3:c.-97C>T	NP_000181.2:n.-97C>T
NM_001258208.1:c.-97C>T	NP_001245137.1:n.-97C>T
NM_001258209.1:c.-239C>T	NP_001245138.1:n.-239C>T
XM_005271531.1:c.-239C>T	XP_005271588.1:n.-239C>T
XM_005271532.1:c.-215C>T	XP_005271589.1:n.-215C>T
XM_005271533.2:c.-97C>T	XP_005271590.1:n.-97C>T
NM_000190.4:c.-97C>T MANE Select	NP_000181.2:n.-97C>T
XM_005271533.3:c.-97C>T	XP_005271590.1:n.-97C>T
XM_024448460.1:c.-97C>T	XP_024304228.1:n.-97C>T
NM_001258208.2:c.-97C>T	NP_001245137.1:n.-97C>T
NM_001258209.2:c.-239C>T	NP_001245138.1:n.-239C>T