Canonical Allele Identifier: CA239560870

Gene: TRHDE

Linked Data

• dbSNP Id: rs536690745
• gnomAD v2: 12-72723966-C-G
• gnomAD v3: 12-72330186-C-G
• gnomAD v4: 12-72330186-C-G
• MyVariant Identifiers: chr12:g.72723966C>G (hg19) ; chr12:g.72330186C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.72330186C>G , CM000674.2:g.72330186C>G	GRCh38
NC_000012.11:g.72723966C>G , CM000674.1:g.72723966C>G	GRCh37
NC_000012.10:g.71010233C>G	NCBI36
NG_046971.1:g.62607C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261180.10:c.1188+43232C>G MANE Select	ENSP00000261180.5:n.1188+43232C>G
ENST00000547300.2:c.1188+43232C>G	ENSP00000447822.2:n.1188+43232C>G
ENST00000261180.9:c.1053+43232C>G	ENSP00000261180.4:n.1053+43232C>G
ENST00000261180.8:c.1053+43232C>G	ENSP00000261180.4:n.1053+43232C>G
ENST00000547300.1:c.349+43232C>G
ENST00000548156.1:n.280-47809C>G
NM_013381.2:c.1053+43232C>G	NP_037513.1:n.1053+43232C>G
XM_005268819.3:c.1188+43232C>G	XP_005268876.1:n.1188+43232C>G
XR_944529.1:n.1251+43232C>G
XM_005268819.5:c.1053+43232C>G	XP_005268876.2:n.1053+43232C>G
XM_017019243.2:c.1053+43232C>G	XP_016874732.2:n.1053+43232C>G
XM_017019244.1:c.144+43232C>G	XP_016874733.1:n.144+43232C>G
NM_013381.3:c.1188+43232C>G MANE Select	NP_037513.2:n.1188+43232C>G