Canonical Allele Identifier: CA2616354558

Gene: HMBS

Linked Data

• gnomAD v4: 11-119092025-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092025T>C , CM000673.2:g.119092025T>C	GRCh38
NC_000011.9:g.118962735T>C , CM000673.1:g.118962735T>C	GRCh37
NC_000011.8:g.118467945T>C	NCBI36
NG_008093.1:g.12149T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.448-100T>C	ENSP00000509288.1:n.448-100T>C
ENST00000691144.1:n.2354-100T>C
ENST00000691249.1:n.1197-100T>C
ENST00000442944.7:c.595-100T>C	ENSP00000392041.3:n.595-100T>C
ENST00000536813.6:c.562-100T>C	ENSP00000438726.2:n.562-100T>C
ENST00000546302.6:c.535-100T>C	ENSP00000445599.1:n.535-100T>C
ENST00000640813.1:c.461+151T>C	ENSP00000491061.1:n.461+151T>C
ENST00000648026.1:c.507-100T>C	ENSP00000498044.1:n.507-100T>C
ENST00000648374.1:c.562-100T>C	ENSP00000497255.1:n.562-100T>C
ENST00000648488.1:c.*86-100T>C	ENSP00000498079.1:n.*86-100T>C
ENST00000649823.1:n.830-100T>C
ENST00000650101.1:c.544-100T>C	ENSP00000496970.1:n.544-100T>C
ENST00000650307.1:n.1439-100T>C
ENST00000652429.1:c.613-100T>C MANE Select	ENSP00000498786.1:n.613-100T>C
ENST00000278715.7:c.613-100T>C	ENSP00000278715.3:n.613-100T>C
ENST00000392841.1:c.562-100T>C	ENSP00000376584.1:n.562-100T>C
ENST00000442944.6:c.562-100T>C	ENSP00000392041.2:n.562-100T>C
ENST00000537841.5:c.562-100T>C	ENSP00000444730.1:n.562-100T>C
ENST00000542044.5:n.1058-100T>C
ENST00000542345.5:n.751-100T>C
ENST00000542729.5:c.562-100T>C	ENSP00000443058.1:n.562-100T>C
ENST00000543090.5:c.559-379T>C	ENSP00000445429.1:n.559-379T>C
ENST00000543543.5:n.848-100T>C
ENST00000544182.1:n.488T>C
ENST00000544387.5:c.613-100T>C	ENSP00000438424.1:n.613-100T>C
ENST00000545621.5:c.*508-100T>C	ENSP00000444849.1:n.*508-100T>C
ENST00000546226.5:n.901-100T>C
ENST00000546302.5:c.535-100T>C	ENSP00000445599.1:n.535-100T>C
NM_000190.3:c.613-100T>C	NP_000181.2:n.613-100T>C
NM_001024382.1:c.562-100T>C	NP_001019553.1:n.562-100T>C
NM_001258208.1:c.613-100T>C	NP_001245137.1:n.613-100T>C
NM_001258209.1:c.562-100T>C	NP_001245138.1:n.562-100T>C
XM_005271531.1:c.562-100T>C	XP_005271588.1:n.562-100T>C
XM_005271532.1:c.562-100T>C	XP_005271589.1:n.562-100T>C
XM_005271533.2:c.559-100T>C	XP_005271590.1:n.559-100T>C
XM_011542796.1:c.448-100T>C	XP_011541098.1:n.448-100T>C
NM_000190.4:c.613-100T>C MANE Select	NP_000181.2:n.613-100T>C
NM_001024382.2:c.562-100T>C	NP_001019553.1:n.562-100T>C
XM_005271533.3:c.559-100T>C	XP_005271590.1:n.559-100T>C
XM_017017629.1:c.562-100T>C	XP_016873118.1:n.562-100T>C
XM_024448460.1:c.559-100T>C	XP_024304228.1:n.559-100T>C
NM_001258208.2:c.613-100T>C	NP_001245137.1:n.613-100T>C
NM_001258209.2:c.562-100T>C	NP_001245138.1:n.562-100T>C