Linked Data
dbSNP Id:
rs35711467
gnomAD v3:
8-1857875-G-GATCTATC
gnomAD v4:
8-1857875-G-GATCTATC
MyVariant Identifiers:
chr8:g.1806041_1806042insATCTATC (hg19)
chr8:g.1857875_1857876insATCTATC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.1857878_1857879insTATCATC , CM000670.2:g.1857878_1857879insTATCATC | GRCh38 |
| NC_000008.10:g.1806044_1806045insTATCATC , CM000670.1:g.1806044_1806045insTATCATC | GRCh37 |
| NC_000008.9:g.1793451_1793452insTATCATC | NCBI36 |
| NG_008480.1:g.38896_38897insTATCATC , LRG_234:g.38896_38897insTATCATC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000349830.8:c.38-82_38-81insTATCATC MANE Select | ENSP00000340297.3:n.38-82_38-81insTATCATC | |
| ENST00000635773.1:c.497-82_497-81insTATCATC | ||
| ENST00000635855.1:c.628-82_628-81insTATCATC | ENSP00000489726.1:n.628-82_628-81insTATCATC | |
| ENST00000636175.1:c.428-82_428-81insTATCATC | ||
| ENST00000349830.7:c.38-82_38-81insTATCATC | ENSP00000340297.3:n.38-82_38-81insTATCATC | |
| ENST00000398564.5:c.110-82_110-81insTATCATC | ENSP00000381571.1:n.110-82_110-81insTATCATC | |
| ENST00000518288.5:c.110-82_110-81insTATCATC | ENSP00000431012.1:n.110-82_110-81insTATCATC | |
| ENST00000520359.5:c.38-82_38-81insTATCATC | ENSP00000427909.1:n.38-82_38-81insTATCATC | |
| NM_001308152.1:c.38-82_38-81insTATCATC | NP_001295081.1:n.38-82_38-81insTATCATC | |
| NM_001308153.1:c.110-82_110-81insTATCATC | NP_001295082.1:n.110-82_110-81insTATCATC | |
| NM_014629.2:c.38-82_38-81insTATCATC , LRG_234t1:c.38-82_38-81insTATCATC | NP_055444.2:n.38-82_38-81insTATCATC | |
| NM_014629.3:c.38-82_38-81insTATCATC | NP_055444.2:n.38-82_38-81insTATCATC | |
| XM_005266041.2:c.38-82_38-81insTATCATC | XP_005266098.1:n.38-82_38-81insTATCATC | |
| XM_011534766.1:c.38-82_38-81insTATCATC | XP_011533068.1:n.38-82_38-81insTATCATC | |
| XM_011534767.1:c.38-82_38-81insTATCATC | XP_011533069.1:n.38-82_38-81insTATCATC | |
| XM_011534768.1:c.38-82_38-81insTATCATC | XP_011533070.1:n.38-82_38-81insTATCATC | |
| XM_011534769.1:c.-8-82_-8-81insTATCATC | XP_011533071.1:n.-8-82_-8-81insTATCATC | |
| XM_011534770.1:c.38-82_38-81insTATCATC | XP_011533072.1:n.38-82_38-81insTATCATC | |
| XM_005266041.4:c.38-82_38-81insTATCATC | XP_005266098.1:n.38-82_38-81insTATCATC | |
| XM_011534767.2:c.38-82_38-81insTATCATC | XP_011533069.1:n.38-82_38-81insTATCATC | |
| XM_011534770.2:c.38-82_38-81insTATCATC | XP_011533072.1:n.38-82_38-81insTATCATC | |
| XM_017014003.1:c.110-82_110-81insTATCATC | XP_016869492.1:n.110-82_110-81insTATCATC | |
| XM_024447334.1:c.38-82_38-81insTATCATC | XP_024303102.1:n.38-82_38-81insTATCATC | |
| XM_024447335.1:c.122-82_122-81insTATCATC | XP_024303103.1:n.122-82_122-81insTATCATC | |
| NM_014629.4:c.38-82_38-81insTATCATC MANE Select | NP_055444.2:n.38-82_38-81insTATCATC | |
| NM_001308152.2:c.38-82_38-81insTATCATC | NP_001295081.1:n.38-82_38-81insTATCATC | |
| NM_001308153.2:c.110-82_110-81insTATCATC | NP_001295082.1:n.110-82_110-81insTATCATC |