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Identifiers and link-outs to other resources
MyVariant Identifiers:
chr13:g.51504829C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.50930693C>G , CM000675.2:g.50930693C>G | GRCh38 |
| NC_000013.10:g.51504829C>G , CM000675.1:g.51504829C>G | GRCh37 |
| NC_000013.9:g.50402830C>G | NCBI36 |
| NG_009055.1:g.25938C>G , LRG_279:g.25938C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NM_001142279.2:c.255C>G , LRG_279t1:c.255C>G | NP_001135751.1:p.Leu85= | |
| NM_024570.3:c.255C>G , LRG_279t2:c.255C>G | NP_078846.2:p.Leu85= | |
| XM_005266524.2:c.255C>G | XP_005266581.1:p.Leu85= | |
| XM_005266525.2:c.255C>G | XP_005266582.1:p.Leu85= | |
| XM_006719867.2:c.237C>G | XP_006719930.1:p.Leu79= | |
| XM_011535229.1:c.255C>G | XP_011533531.1:p.Leu85= | |
| XM_011535230.1:c.255C>G | XP_011533532.1:p.Leu85= | |
| XM_011535231.1:c.255C>G | XP_011533533.1:p.Leu85= | |
| XM_011535232.1:c.93C>G | XP_011533534.1:p.Leu31= | |
| XM_011535233.1:c.-359C>G | XP_011533535.1:p.= | |
| XM_011535234.1:c.255C>G | XP_011533536.1:p.Leu85= | |
| XM_006719867.4:c.237C>G | XP_006719930.1:p.Leu79= | |
| XM_011535230.2:c.255C>G | XP_011533532.1:p.Leu85= | |
| XM_011535231.2:c.255C>G | XP_011533533.1:p.Leu85= | |
| XM_011535233.2:c.-359C>G | XP_011533535.1:p.= | |
| XM_017020747.1:c.255C>G | XP_016876236.1:p.Leu85= | |
| ENST00000336617.7:c.255C>G | ENSP00000337623.2:p.Leu85= | |
| ENST00000422660.5:c.255C>G | ENSP00000389877.1:p.Leu85= | |
| ENST00000459681.2:n.53C>G | ||
| ENST00000495244.6:n.266C>G | ||
| ENST00000611510.4:c.255C>G | ENSP00000481236.2:p.Leu85= |