Canonical Allele Identifier: CA857153338

Gene: INTS8

Linked Data

• dbSNP Id: rs1483031011
• gnomAD v3: 8-94827657-T-C
• gnomAD v4: 8-94827657-T-C
• MyVariant Identifiers: chr8:g.95839885T>C (hg19) ; chr8:g.94827657T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.94827657T>C , CM000670.2:g.94827657T>C	GRCh38
NC_000008.10:g.95839885T>C , CM000670.1:g.95839885T>C	GRCh37
NC_000008.9:g.95909061T>C	NCBI36
NG_047163.1:g.19347T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000523731.6:c.447-65T>C MANE Select	ENSP00000430338.1:n.447-65T>C
ENST00000343161.8:c.447-65T>C	ENSP00000343274.4:n.447-65T>C
ENST00000519053.5:c.120-65T>C	ENSP00000429056.1:n.120-65T>C
ENST00000519457.5:c.306-65T>C	ENSP00000428260.1:n.306-65T>C
ENST00000521860.5:c.409-65T>C
ENST00000522171.5:c.324-65T>C	ENSP00000429340.1:n.324-65T>C
ENST00000523206.5:c.447-65T>C	ENSP00000429452.1:n.447-65T>C
ENST00000523321.5:n.572-65T>C
ENST00000523731.5:c.447-65T>C	ENSP00000430338.1:n.447-65T>C
ENST00000524333.5:c.447-65T>C	ENSP00000427840.1:n.447-65T>C
NM_017864.3:c.447-65T>C	NP_060334.2:n.447-65T>C
NR_073444.1:n.589-65T>C
NR_073445.1:n.589-65T>C
XM_006716602.2:c.447-65T>C	XP_006716665.1:n.447-65T>C
XM_006716603.2:c.120-65T>C	XP_006716666.1:n.120-65T>C
XM_011517155.1:c.324-65T>C	XP_011515457.1:n.324-65T>C
XM_011517156.1:c.447-65T>C	XP_011515458.1:n.447-65T>C
XM_011517157.1:c.120-65T>C	XP_011515459.1:n.120-65T>C
XM_017013616.1:c.447-65T>C	XP_016869105.1:n.447-65T>C
XM_017013617.1:c.447-65T>C	XP_016869106.1:n.447-65T>C
XM_017013618.1:c.120-65T>C	XP_016869107.1:n.120-65T>C
XM_017013619.1:c.-837-65T>C	XP_016869108.1:n.-837-65T>C
NM_017864.4:c.447-65T>C MANE Select	NP_060334.2:n.447-65T>C
NR_073444.2:n.592-65T>C
NR_073445.2:n.592-65T>C