Canonical Allele Identifier: CA6313998

Gene: HMBS

Linked Data

• dbSNP Id: rs749426688
• ExAC: 11:118960359 C / T
• gnomAD v2: 11-118960359-C-T
• gnomAD v3: 11-119089649-C-T
• gnomAD v4: 11-119089649-C-T
• MyVariant Identifiers: chr11:g.118960359C>T (hg19) ; chr11:g.119089649C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119089649C>T , CM000673.2:g.119089649C>T	GRCh38
NC_000011.9:g.118960359C>T , CM000673.1:g.118960359C>T	GRCh37
NC_000011.8:g.118465569C>T	NCBI36
NG_008093.1:g.9773C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000686218.1:c.102-34C>T	ENSP00000509288.1:n.102-34C>T
ENST00000686690.1:n.888-34C>T
ENST00000691144.1:n.2008-34C>T
ENST00000691249.1:n.851-34C>T
ENST00000442944.7:c.249-34C>T	ENSP00000392041.3:n.249-34C>T
ENST00000534956.2:n.216-34C>T
ENST00000536813.6:c.216-34C>T	ENSP00000438726.2:n.216-34C>T
ENST00000546302.6:c.267-341C>T	ENSP00000445599.1:n.267-341C>T
ENST00000640813.1:c.216-34C>T	ENSP00000491061.1:n.216-34C>T
ENST00000648026.1:c.261-34C>T	ENSP00000498044.1:n.261-34C>T
ENST00000648374.1:c.216-34C>T	ENSP00000497255.1:n.216-34C>T
ENST00000648488.1:c.216-34C>T	ENSP00000498079.1:n.216-34C>T
ENST00000649823.1:n.484-34C>T
ENST00000649868.1:c.122-34C>T	ENSP00000497548.1:n.122-34C>T
ENST00000650101.1:c.198-34C>T	ENSP00000496970.1:n.198-34C>T
ENST00000650307.1:n.1093-34C>T
ENST00000652429.1:c.267-34C>T MANE Select	ENSP00000498786.1:n.267-34C>T
ENST00000278715.7:c.267-34C>T	ENSP00000278715.3:n.267-34C>T
ENST00000392841.1:c.216-34C>T	ENSP00000376584.1:n.216-34C>T
ENST00000442944.6:c.216-34C>T	ENSP00000392041.2:n.216-34C>T
ENST00000534956.1:n.183-34C>T
ENST00000535253.5:c.216-34C>T	ENSP00000442079.1:n.216-34C>T
ENST00000535793.5:c.*162-34C>T	ENSP00000439904.1:n.*162-34C>T
ENST00000536185.5:n.385-34C>T
ENST00000536813.5:c.249-34C>T	ENSP00000438726.1:n.249-34C>T
ENST00000537841.5:c.216-34C>T	ENSP00000444730.1:n.216-34C>T
ENST00000539986.5:c.216-34C>T	ENSP00000440092.1:n.216-34C>T
ENST00000542044.5:n.712-34C>T
ENST00000542345.5:n.405-34C>T
ENST00000542729.5:c.216-34C>T	ENSP00000443058.1:n.216-34C>T
ENST00000542822.5:c.*203-34C>T	ENSP00000444817.1:n.*203-34C>T
ENST00000543090.5:c.213-34C>T	ENSP00000445429.1:n.213-34C>T
ENST00000543543.5:n.502-34C>T
ENST00000543821.5:n.413-34C>T
ENST00000544360.5:n.235-34C>T
ENST00000544387.5:c.267-34C>T	ENSP00000438424.1:n.267-34C>T
ENST00000545621.5:c.*162-34C>T	ENSP00000444849.1:n.*162-34C>T
ENST00000546226.5:n.326-34C>T
ENST00000546302.5:c.267-341C>T	ENSP00000445599.1:n.267-341C>T
NM_000190.3:c.267-34C>T	NP_000181.2:n.267-34C>T
NM_001024382.1:c.216-34C>T	NP_001019553.1:n.216-34C>T
NM_001258208.1:c.267-34C>T	NP_001245137.1:n.267-34C>T
NM_001258209.1:c.216-34C>T	NP_001245138.1:n.216-34C>T
XM_005271531.1:c.216-34C>T	XP_005271588.1:n.216-34C>T
XM_005271532.1:c.216-34C>T	XP_005271589.1:n.216-34C>T
XM_005271533.2:c.213-34C>T	XP_005271590.1:n.213-34C>T
XM_011542796.1:c.102-34C>T	XP_011541098.1:n.102-34C>T
NM_000190.4:c.267-34C>T MANE Select	NP_000181.2:n.267-34C>T
NM_001024382.2:c.216-34C>T	NP_001019553.1:n.216-34C>T
XM_005271533.3:c.213-34C>T	XP_005271590.1:n.213-34C>T
XM_017017629.1:c.216-34C>T	XP_016873118.1:n.216-34C>T
XM_024448460.1:c.213-34C>T	XP_024304228.1:n.213-34C>T
NM_001258208.2:c.267-34C>T	NP_001245137.1:n.267-34C>T
NM_001258209.2:c.216-34C>T	NP_001245138.1:n.216-34C>T