Canonical Allele Identifier: CA907588459

Gene: TMIE

Linked Data

• dbSNP Id: rs1365571961
• gnomAD v3: 3-46705732-A-G
• gnomAD v4: 3-46705732-A-G
• MyVariant Identifiers: chr3:g.46747222A>G (hg19) ; chr3:g.46705732A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46705732A>G , CM000665.2:g.46705732A>G	GRCh38
NC_000003.11:g.46747222A>G , CM000665.1:g.46747222A>G	GRCh37
NC_000003.10:g.46722226A>G	NCBI36
NG_011628.1:g.9400A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643606.3:c.94-58A>G MANE Select	ENSP00000494576.2:n.94-58A>G
ENST00000644830.1:c.-66-58A>G	ENSP00000495111.1:n.-66-58A>G
ENST00000326431.3:c.94-58A>G	ENSP00000324775.3:n.94-58A>G
NM_147196.2:c.94-58A>G	NP_671729.2:n.94-58A>G
XM_006713097.2:c.-66-58A>G	XP_006713160.1:n.-66-58A>G
XM_011533574.1:c.-66-58A>G	XP_011531876.1:n.-66-58A>G
XM_006713097.4:c.-66-58A>G	XP_006713160.1:n.-66-58A>G
XM_024453446.1:c.-66-58A>G	XP_024309214.1:n.-66-58A>G
NM_001370524.1:c.-66-58A>G	NP_001357453.1:n.-66-58A>G
NM_001370525.1:c.-66-58A>G	NP_001357454.1:n.-66-58A>G
NM_147196.3:c.94-58A>G MANE Select	NP_671729.2:n.94-58A>G