Canonical Allele Identifier: CA2003782961

Gene: HMBS

Linked Data

• dbSNP Id: rs1946203091
• gnomAD v4: 11-119090124-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119090124G>A , CM000673.2:g.119090124G>A	GRCh38
NC_000011.9:g.118960834G>A , CM000673.1:g.118960834G>A	GRCh37
NC_000011.8:g.118466044G>A	NCBI36
NG_008093.1:g.10248G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000686218.1:c.257+57G>A	ENSP00000509288.1:n.257+57G>A
ENST00000686690.1:n.1272+57G>A
ENST00000691144.1:n.2163+57G>A
ENST00000691249.1:n.1006+57G>A
ENST00000442944.7:c.404+57G>A	ENSP00000392041.3:n.404+57G>A
ENST00000534956.2:n.371+57G>A
ENST00000536813.6:c.371+57G>A	ENSP00000438726.2:n.371+57G>A
ENST00000546302.6:c.344+57G>A	ENSP00000445599.1:n.344+57G>A
ENST00000640813.1:c.371+57G>A	ENSP00000491061.1:n.371+57G>A
ENST00000648026.1:c.416+57G>A	ENSP00000498044.1:n.416+57G>A
ENST00000648374.1:c.371+57G>A	ENSP00000497255.1:n.371+57G>A
ENST00000648488.1:c.371+57G>A	ENSP00000498079.1:n.371+57G>A
ENST00000649823.1:n.639+57G>A
ENST00000649868.1:c.*130+57G>A	ENSP00000497548.1:n.*130+57G>A
ENST00000650101.1:c.353+57G>A	ENSP00000496970.1:n.353+57G>A
ENST00000650307.1:n.1248+57G>A
ENST00000652429.1:c.422+57G>A MANE Select	ENSP00000498786.1:n.422+57G>A
ENST00000278715.7:c.422+57G>A	ENSP00000278715.3:n.422+57G>A
ENST00000392841.1:c.371+57G>A	ENSP00000376584.1:n.371+57G>A
ENST00000442944.6:c.371+57G>A	ENSP00000392041.2:n.371+57G>A
ENST00000534956.1:n.338+57G>A
ENST00000535253.5:c.371+57G>A	ENSP00000442079.1:n.371+57G>A
ENST00000535793.5:c.*317+57G>A	ENSP00000439904.1:n.*317+57G>A
ENST00000537841.5:c.371+57G>A	ENSP00000444730.1:n.371+57G>A
ENST00000539986.5:c.371+57G>A	ENSP00000440092.1:n.371+57G>A
ENST00000542044.5:n.867+57G>A
ENST00000542345.5:n.560+57G>A
ENST00000542729.5:c.371+57G>A	ENSP00000443058.1:n.371+57G>A
ENST00000542822.5:c.*358+57G>A	ENSP00000444817.1:n.*358+57G>A
ENST00000543090.5:c.368+57G>A	ENSP00000445429.1:n.368+57G>A
ENST00000543543.5:n.657+57G>A
ENST00000544360.5:n.390+57G>A
ENST00000544387.5:c.422+57G>A	ENSP00000438424.1:n.422+57G>A
ENST00000545621.5:c.*317+57G>A	ENSP00000444849.1:n.*317+57G>A
ENST00000546226.5:n.710+57G>A
ENST00000546302.5:c.344+57G>A	ENSP00000445599.1:n.344+57G>A
NM_000190.3:c.422+57G>A	NP_000181.2:n.422+57G>A
NM_001024382.1:c.371+57G>A	NP_001019553.1:n.371+57G>A
NM_001258208.1:c.422+57G>A	NP_001245137.1:n.422+57G>A
NM_001258209.1:c.371+57G>A	NP_001245138.1:n.371+57G>A
XM_005271531.1:c.371+57G>A	XP_005271588.1:n.371+57G>A
XM_005271532.1:c.371+57G>A	XP_005271589.1:n.371+57G>A
XM_005271533.2:c.368+57G>A	XP_005271590.1:n.368+57G>A
XM_011542796.1:c.257+57G>A	XP_011541098.1:n.257+57G>A
NM_000190.4:c.422+57G>A MANE Select	NP_000181.2:n.422+57G>A
NM_001024382.2:c.371+57G>A	NP_001019553.1:n.371+57G>A
XM_005271533.3:c.368+57G>A	XP_005271590.1:n.368+57G>A
XM_017017629.1:c.371+57G>A	XP_016873118.1:n.371+57G>A
XM_024448460.1:c.368+57G>A	XP_024304228.1:n.368+57G>A
NM_001258208.2:c.422+57G>A	NP_001245137.1:n.422+57G>A
NM_001258209.2:c.371+57G>A	NP_001245138.1:n.371+57G>A