Canonical Allele Identifier: CA6314137

Gene: HMBS

Linked Data

• dbSNP Id: rs771276134
• ExAC: 11:118962938 T / G
• gnomAD v2: 11-118962938-T-G
• gnomAD v4: 11-119092228-T-G
• MyVariant Identifiers: chr11:g.118962938T>G (hg19) ; chr11:g.119092228T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092228T>G , CM000673.2:g.119092228T>G	GRCh38
NC_000011.9:g.118962938T>G , CM000673.1:g.118962938T>G	GRCh37
NC_000011.8:g.118468148T>G	NCBI36
NG_008093.1:g.12352T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.486+65T>G	ENSP00000509288.1:n.486+65T>G
ENST00000691144.1:n.2457T>G
ENST00000691249.1:n.1300T>G
ENST00000442944.7:c.633+65T>G	ENSP00000392041.3:n.633+65T>G
ENST00000536813.6:c.600+65T>G	ENSP00000438726.2:n.600+65T>G
ENST00000640813.1:c.462-176T>G	ENSP00000491061.1:n.462-176T>G
ENST00000648026.1:c.545+65T>G	ENSP00000498044.1:n.545+65T>G
ENST00000648374.1:c.600+65T>G	ENSP00000497255.1:n.600+65T>G
ENST00000649823.1:n.933T>G
ENST00000650101.1:c.582+65T>G	ENSP00000496970.1:n.582+65T>G
ENST00000650307.1:n.1477+65T>G
ENST00000652429.1:c.651+65T>G MANE Select	ENSP00000498786.1:n.651+65T>G
ENST00000278715.7:c.651+65T>G	ENSP00000278715.3:n.651+65T>G
ENST00000392841.1:c.600+65T>G	ENSP00000376584.1:n.600+65T>G
ENST00000442944.6:c.600+65T>G	ENSP00000392041.2:n.600+65T>G
ENST00000537841.5:c.600+65T>G	ENSP00000444730.1:n.600+65T>G
ENST00000542044.5:n.1096+65T>G
ENST00000542345.5:n.854T>G
ENST00000542729.5:c.600+65T>G	ENSP00000443058.1:n.600+65T>G
ENST00000543090.5:c.559-176T>G	ENSP00000445429.1:n.559-176T>G
ENST00000543543.5:n.951T>G
ENST00000544182.1:n.691T>G
ENST00000544387.5:c.651+65T>G	ENSP00000438424.1:n.651+65T>G
ENST00000545621.5:c.*611T>G	ENSP00000444849.1:n.*611T>G
ENST00000546226.5:n.1004T>G
NM_000190.3:c.651+65T>G	NP_000181.2:n.651+65T>G
NM_001024382.1:c.600+65T>G	NP_001019553.1:n.600+65T>G
NM_001258208.1:c.651+65T>G	NP_001245137.1:n.651+65T>G
NM_001258209.1:c.600+65T>G	NP_001245138.1:n.600+65T>G
XM_005271531.1:c.600+65T>G	XP_005271588.1:n.600+65T>G
XM_005271532.1:c.600+65T>G	XP_005271589.1:n.600+65T>G
XM_005271533.2:c.597+65T>G	XP_005271590.1:n.597+65T>G
XM_011542796.1:c.486+65T>G	XP_011541098.1:n.486+65T>G
NM_000190.4:c.651+65T>G MANE Select	NP_000181.2:n.651+65T>G
NM_001024382.2:c.600+65T>G	NP_001019553.1:n.600+65T>G
XM_005271533.3:c.597+65T>G	XP_005271590.1:n.597+65T>G
XM_017017629.1:c.600+65T>G	XP_016873118.1:n.600+65T>G
XM_024448460.1:c.597+65T>G	XP_024304228.1:n.597+65T>G
NM_001258208.2:c.651+65T>G	NP_001245137.1:n.651+65T>G
NM_001258209.2:c.600+65T>G	NP_001245138.1:n.600+65T>G