Linked Data
MyVariant Identifiers:
chr2:g.203329626A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.202464903A>C , CM000664.2:g.202464903A>C | GRCh38 |
| NC_000002.11:g.203329626A>C , CM000664.1:g.203329626A>C | GRCh37 |
| NC_000002.10:g.203037871A>C | NCBI36 |
| NG_009363.1:g.93577A>C , LRG_712:g.93577A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374580.10:c.171A>C MANE Select | ENSP00000363708.4:p.Thr57= | |
| ENST00000638587.1:c.96A>C | ENSP00000491062.1:p.Thr32= | |
| ENST00000374574.2:c.171A>C | ENSP00000363702.2:p.Thr57= | |
| ENST00000374580.8:c.171A>C | ENSP00000363708.4:p.Thr57= | |
| ENST00000479069.1:n.78A>C | ||
| NM_001204.6:c.171A>C , LRG_712t1:c.171A>C | NP_001195.2:p.Thr57= | |
| XM_011511687.1:c.171A>C | XP_011509989.1:p.Thr57= | |
| XM_011511688.1:c.171A>C | XP_011509990.1:p.Thr57= | |
| NM_001204.7:c.171A>C MANE Select | NP_001195.2:p.Thr57= |