Linked Data
dbSNP Id:
rs1969882553
gnomAD v4:
19-44909077-C-T
MyVariant Identifiers:
chr19:g.45412334C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.44909077C>T , CM000681.2:g.44909077C>T | GRCh38 |
| NC_000019.9:g.45412334C>T , CM000681.1:g.45412334C>T | GRCh37 |
| NC_000019.8:g.50104174C>T | NCBI36 |
| NG_007084.2:g.8296C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000252486.9:c.781C>T MANE Select | ENSP00000252486.3:p.Leu261= | |
| ENST00000252486.8:c.781C>T | ENSP00000252486.3:p.Leu261= | |
| NM_000041.3:c.781C>T | NP_000032.1:p.Leu261= | |
| NM_001302688.1:c.859C>T | NP_001289617.1:p.Leu287= | |
| NM_001302689.1:c.781C>T | NP_001289618.1:p.Leu261= | |
| NM_001302690.1:c.781C>T | NP_001289619.1:p.Leu261= | |
| NM_001302691.1:c.781C>T | NP_001289620.1:p.Leu261= | |
| NM_000041.4:c.781C>T MANE Select | NP_000032.1:p.Leu261= | |
| NM_001302688.2:c.859C>T | NP_001289617.1:p.Leu287= | |
| NM_001302689.2:c.781C>T | NP_001289618.1:p.Leu261= | |
| NM_001302691.2:c.781C>T | NP_001289620.1:p.Leu261= | |
| NM_001302690.2:c.781C>T | NP_001289619.1:p.Leu261= |