Linked Data
dbSNP Id:
rs1822067312
gnomAD v4:
8-144414330-G-A
MyVariant Identifiers:
chr8:g.145639714G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.144414330G>A , CM000670.2:g.144414330G>A | GRCh38 |
| NC_000008.10:g.145639714G>A , CM000670.1:g.145639714G>A | GRCh37 |
| NC_000008.9:g.145610522G>A | NCBI36 |
| NG_012234.2:g.7561C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301305.8:c.1081C>T MANE Select | ENSP00000301305.4:p.Leu361= | |
| ENST00000276833.9:c.1006C>T | ENSP00000276833.5:p.Leu336= | |
| ENST00000301305.7:c.1081C>T | ENSP00000301305.3:p.Leu361= | |
| NM_017767.2:c.1006C>T | NP_060237.2:p.Leu336= | |
| NM_130849.3:c.1081C>T | NP_570901.2:p.Leu361= | |
| XM_006716599.1:c.1081C>T | XP_006716662.1:p.Leu361= | |
| XM_011517153.1:c.799C>T | XP_011515455.1:p.Leu267= | |
| XM_024447188.1:c.799C>T | XP_024302956.1:p.Leu267= | |
| XM_024447189.1:c.799C>T | XP_024302957.1:p.Leu267= | |
| NM_001374839.1:c.799C>T | NP_001361768.1:p.Leu267= | |
| NM_017767.3:c.1006C>T | NP_060237.3:p.Leu336= | |
| NM_130849.4:c.1081C>T MANE Select | NP_570901.3:p.Leu361= |