Canonical Allele Identifier: CA73730176

Gene: TMIE

Linked Data

• dbSNP Id: rs750976116
• gnomAD v4: 3-46705749-T-G
• MyVariant Identifiers: chr3:g.46747239T>G (hg19) ; chr3:g.46705749T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46705749T>G , CM000665.2:g.46705749T>G	GRCh38
NC_000003.11:g.46747239T>G , CM000665.1:g.46747239T>G	GRCh37
NC_000003.10:g.46722243T>G	NCBI36
NG_011628.1:g.9417T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643606.3:c.94-41T>G MANE Select	ENSP00000494576.2:n.94-41T>G
ENST00000644830.1:c.-66-41T>G	ENSP00000495111.1:n.-66-41T>G
ENST00000326431.3:c.94-41T>G	ENSP00000324775.3:n.94-41T>G
NM_147196.2:c.94-41T>G	NP_671729.2:n.94-41T>G
XM_006713097.2:c.-66-41T>G	XP_006713160.1:n.-66-41T>G
XM_011533574.1:c.-66-41T>G	XP_011531876.1:n.-66-41T>G
XM_006713097.4:c.-66-41T>G	XP_006713160.1:n.-66-41T>G
XM_024453446.1:c.-66-41T>G	XP_024309214.1:n.-66-41T>G
NM_001370524.1:c.-66-41T>G	NP_001357453.1:n.-66-41T>G
NM_001370525.1:c.-66-41T>G	NP_001357454.1:n.-66-41T>G
NM_147196.3:c.94-41T>G MANE Select	NP_671729.2:n.94-41T>G