Canonical Allele Identifier: CA1362233076
Gene: TMIE HGNC NCBI

Linked Data

dbSNP Id: rs7635402
gnomAD v4: 3-46705765-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46705765C>A , CM000665.2:g.46705765C>A GRCh38
NC_000003.11:g.46747255C>A , CM000665.1:g.46747255C>A GRCh37
NC_000003.10:g.46722259C>A NCBI36
NG_011628.1:g.9433C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000643606.3:c.94-25C>A MANE Select ENSP00000494576.2:n.94-25C>A
ENST00000644830.1:c.-66-25C>A ENSP00000495111.1:n.-66-25C>A
ENST00000326431.3:c.94-25C>A ENSP00000324775.3:n.94-25C>A
NM_147196.2:c.94-25C>A NP_671729.2:n.94-25C>A
XM_006713097.2:c.-66-25C>A XP_006713160.1:n.-66-25C>A
XM_011533574.1:c.-66-25C>A XP_011531876.1:n.-66-25C>A
XM_006713097.4:c.-66-25C>A XP_006713160.1:n.-66-25C>A
XM_024453446.1:c.-66-25C>A XP_024309214.1:n.-66-25C>A
NM_001370524.1:c.-66-25C>A NP_001357453.1:n.-66-25C>A
NM_001370525.1:c.-66-25C>A NP_001357454.1:n.-66-25C>A
NM_147196.3:c.94-25C>A MANE Select NP_671729.2:n.94-25C>A