Linked Data
ClinVar Variation Id:
1082690
ClinVar RCV Id:
RCV001399080
dbSNP Id:
rs2132651658
gnomAD v4:
8-27463339-C-T
MyVariant Identifiers:
chr8:g.27320856C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.27463339C>T , CM000670.2:g.27463339C>T | GRCh38 |
| NC_000008.10:g.27320856C>T , CM000670.1:g.27320856C>T | GRCh37 |
| NC_000008.9:g.27376773C>T | NCBI36 |
| NG_015827.1:g.20958G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000407991.3:c.1104G>A MANE Select | ENSP00000385026.1:p.Gly368= | |
| ENST00000240132.7:c.1059G>A | ENSP00000240132.2:p.Gly353= | |
| ENST00000407991.2:c.1104G>A | ENSP00000385026.1:p.Gly368= | |
| ENST00000520600.1:n.290-1585G>A | ||
| ENST00000520933.7:c.1038G>A | ENSP00000429616.2:p.Gly346= | |
| ENST00000523695.5:c.*506G>A | ENSP00000430612.1:n.*506G>A | |
| NM_000742.3:c.1104G>A | NP_000733.2:p.Gly368= | |
| NM_001282455.1:c.1059G>A | NP_001269384.1:p.Gly353= | |
| XM_005273397.1:c.627G>A | XP_005273454.1:p.Gly209= | |
| XM_006716282.1:c.1104G>A | XP_006716345.1:p.Gly368= | |
| XM_011544388.1:c.1104G>A | XP_011542690.1:p.Gly368= | |
| XM_011544389.1:c.510G>A | XP_011542691.1:p.Gly170= | |
| NM_001347705.1:c.627G>A | NP_001334634.1:p.Gly209= | |
| NM_001347706.1:c.627G>A | NP_001334635.1:p.Gly209= | |
| NM_001347707.1:c.510G>A | NP_001334636.1:p.Gly170= | |
| NM_001347708.1:c.510G>A | NP_001334637.1:p.Gly170= | |
| XM_011544389.2:c.510G>A | XP_011542691.1:p.Gly170= | |
| NM_000742.4:c.1104G>A MANE Select | NP_000733.2:p.Gly368= | |
| NM_001282455.2:c.1059G>A | NP_001269384.1:p.Gly353= | |
| NM_001347705.2:c.627G>A | NP_001334634.1:p.Gly209= | |
| NM_001347706.2:c.627G>A | NP_001334635.1:p.Gly209= | |
| NM_001347707.2:c.510G>A | NP_001334636.1:p.Gly170= | |
| NM_001347708.2:c.510G>A | NP_001334637.1:p.Gly170= |