Canonical Allele Identifier: CA73730727

Gene: TMIE

Linked Data

• dbSNP Id: rs749291346
• gnomAD v2: 3-46747774-C-G
• MyVariant Identifiers: chr3:g.46747774C>G (hg19) ; chr3:g.46706284C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46706284C>G , CM000665.2:g.46706284C>G	GRCh38
NC_000003.11:g.46747774C>G , CM000665.1:g.46747774C>G	GRCh37
NC_000003.10:g.46722778C>G	NCBI36
NG_011628.1:g.9952C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643606.3:c.211+377C>G MANE Select	ENSP00000494576.2:n.211+377C>G
ENST00000644830.1:c.52+377C>G	ENSP00000495111.1:n.52+377C>G
ENST00000651652.1:c.109+377C>G	ENSP00000498953.1:n.109+377C>G
ENST00000326431.3:c.211+377C>G	ENSP00000324775.3:n.211+377C>G
NM_147196.2:c.211+377C>G	NP_671729.2:n.211+377C>G
XM_006713097.2:c.52+377C>G	XP_006713160.1:n.52+377C>G
XM_011533574.1:c.52+377C>G	XP_011531876.1:n.52+377C>G
XM_006713097.4:c.52+377C>G	XP_006713160.1:n.52+377C>G
XM_024453446.1:c.52+377C>G	XP_024309214.1:n.52+377C>G
NM_001370524.1:c.52+377C>G	NP_001357453.1:n.52+377C>G
NM_001370525.1:c.52+377C>G	NP_001357454.1:n.52+377C>G
NM_147196.3:c.211+377C>G MANE Select	NP_671729.2:n.211+377C>G