MyVariant.info:
GRCh37
chr2:g.163133446T>C
ClinVar RCV:
ClinVar Variation:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.162276936T>C , CM000664.2:g.162276936T>C | GRCh38 |
| NC_000002.11:g.163133446T>C , CM000664.1:g.163133446T>C | GRCh37 |
| NC_000002.10:g.162841692T>C | NCBI36 |
| NG_011495.1:g.46594A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000697291.1:c.*1652A>G | ENSP00000513228.1:n.*1652A>G | |
| ENST00000648433.1:c.1938A>G | ENSP00000496816.1:p.Lys646= | |
| ENST00000649554.1:n.1665A>G | ||
| ENST00000649979.2:c.2055A>G MANE Select | ENSP00000497271.1:p.Lys685= | |
| ENST00000679938.1:c.1743A>G | ENSP00000505518.1:p.Lys581= | |
| ENST00000263642.2:c.2055A>G | ENSP00000263642.2:p.Lys685= | |
| NM_022168.3:c.2055A>G | NP_071451.2:p.Lys685= | |
| XM_011511628.1:c.1338A>G | XP_011509930.1:p.Lys446= | |
| NM_022168.4:c.2055A>G MANE Select | NP_071451.2:p.Lys685= |