MyVariant.info:
GRCh38
chr18:g.74521017A>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.74521017A>T , CM000680.2:g.74521017A>T | GRCh38 |
| NC_000018.9:g.72188252A>T , CM000680.1:g.72188252A>T | GRCh37 |
| NC_000018.8:g.70339232A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000324262.9:c.*949A>T MANE Select | ENSP00000325548.4:n.*949A>T | |
| ENST00000324262.8:c.*949A>T | ENSP00000325548.4:n.*949A>T | |
| ENST00000324301.12:c.*949A>T | ENSP00000325756.8:n.*949A>T | |
| ENST00000579624.1:c.1089A>T | ENSP00000462034.1:n.1089A>T | |
| ENST00000579847.5:c.*949A>T | ENSP00000462311.1:n.*949A>T | |
| ENST00000584581.5:n.4419A>T | ||
| NM_001168499.1:c.*949A>T | NP_001161971.1:n.*949A>T | |
| NM_018235.2:c.*949A>T | NP_060705.2:n.*949A>T | |
| XM_005266728.1:c.*949A>T | XP_005266785.1:n.*949A>T | |
| XM_006722503.1:c.*949A>T | XP_006722566.1:n.*949A>T | |
| XM_011526071.1:c.*949A>T | XP_011524373.1:n.*949A>T | |
| XM_011526072.1:c.*949A>T | XP_011524374.1:n.*949A>T | |
| XM_011526073.1:c.*949A>T | XP_011524375.1:n.*949A>T | |
| XM_005266728.3:c.*949A>T | XP_005266785.1:n.*949A>T | |
| XM_006722503.2:c.*949A>T | XP_006722566.1:n.*949A>T | |
| XM_011526072.2:c.*949A>T | XP_011524374.1:n.*949A>T | |
| XM_011526073.3:c.*949A>T | XP_011524375.1:n.*949A>T | |
| NM_018235.3:c.*949A>T MANE Select | NP_060705.2:n.*949A>T | |
| NM_001370248.1:c.*949A>T | NP_001357177.1:n.*949A>T | |
| NM_001370249.1:c.*949A>T | NP_001357178.1:n.*949A>T | |
| NM_001370250.1:c.*949A>T | NP_001357179.1:n.*949A>T | |
| NM_001370254.1:c.*949A>T | NP_001357183.1:n.*949A>T | |
| NM_001168499.2:c.*949A>T | NP_001161971.1:n.*949A>T |