Canonical Allele Identifier: CA658933491

Gene: BTRC

Linked Data

• dbSNP Id: rs1452953172
• gnomAD v4: 10-101553875-T-G
• MyVariant Identifiers: chr10:g.103313632T>G (hg19) ; chr10:g.101553875T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101553875T>G , CM000672.2:g.101553875T>G	GRCh38
NC_000010.10:g.103313632T>G , CM000672.1:g.103313632T>G	GRCh37
NC_000010.9:g.103303622T>G	NCBI36
NG_009234.1:g.204808T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370187.8:c.*752T>G MANE Select	ENSP00000359206.3:n.*752T>G
ENST00000370187.7:c.*752T>G	ENSP00000359206.3:n.*752T>G
ENST00000393441.8:c.*752T>G	ENSP00000377088.5:n.*752T>G
ENST00000408038.6:c.*752T>G	ENSP00000385339.2:n.*752T>G
NM_001256856.1:c.*752T>G	NP_001243785.1:n.*752T>G
NM_003939.4:c.*752T>G	NP_003930.1:n.*752T>G
NM_033637.3:c.*752T>G	NP_378663.1:n.*752T>G
XM_005270264.2:c.*752T>G	XP_005270321.1:n.*752T>G
XM_006718054.2:c.*752T>G	XP_006718117.1:n.*752T>G
XM_011540320.1:c.*752T>G	XP_011538622.1:n.*752T>G
XM_011540320.2:c.*752T>G	XP_011538622.1:n.*752T>G
XM_017016870.1:c.*752T>G	XP_016872359.1:n.*752T>G
XM_017016871.1:c.*752T>G	XP_016872360.1:n.*752T>G
XM_017016872.1:c.*752T>G	XP_016872361.1:n.*752T>G
XM_017016873.2:c.*752T>G	XP_016872362.1:n.*752T>G
XM_017016874.1:c.*752T>G	XP_016872363.1:n.*752T>G
XM_024448246.1:c.*752T>G	XP_024304014.1:n.*752T>G
XM_024448247.1:c.*752T>G	XP_024304015.1:n.*752T>G
XR_001747256.1:n.2921T>G
NM_033637.4:c.*752T>G MANE Select	NP_378663.1:n.*752T>G
NM_003939.5:c.*752T>G	NP_003930.1:n.*752T>G
NM_001256856.2:c.*752T>G	NP_001243785.1:n.*752T>G