Linked Data
dbSNP Id:
rs778747295
ExAC:
5:37052537 C / G
gnomAD v2:
5-37052537-C-G
gnomAD v4:
5-37052435-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.37052435C>G , CM000667.2:g.37052435C>G | GRCh38 |
| NC_000005.9:g.37052537C>G , CM000667.1:g.37052537C>G | GRCh37 |
| NC_000005.8:g.37088294C>G | NCBI36 |
| NG_006987.1:g.180553C>G | |
| NG_006987.2:g.180553C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282516.13:c.7132C>G MANE Select | ENSP00000282516.8:p.Pro2378Ala | |
| ENST00000652901.1:c.7132C>G | ENSP00000499536.1:p.Pro2378Ala | |
| ENST00000282516.12:c.7132C>G | ENSP00000282516.8:p.Pro2378Ala | |
| ENST00000448238.2:c.7132C>G | ENSP00000406266.2:p.Pro2378Ala | |
| ENST00000514335.1:n.1014C>G | ||
| ENST00000621733.1:c.1-12143C>G | ENSP00000480694.1:n.1-12143C>G | |
| NM_015384.4:c.7132C>G | NP_056199.2:p.Pro2378Ala | |
| NM_133433.3:c.7132C>G | NP_597677.2:p.Pro2378Ala | |
| XM_005248280.2:c.7132C>G | XP_005248337.1:p.Pro2378Ala | |
| XM_005248282.3:c.6388C>G | XP_005248339.2:p.Pro2130Ala | |
| XM_006714467.2:c.7132C>G | XP_006714530.1:p.Pro2378Ala | |
| XM_006714468.1:c.6934C>G | XP_006714531.1:p.Pro2312Ala | |
| XM_011514014.1:c.6751C>G | XP_011512316.1:p.Pro2251Ala | |
| XM_011514015.1:c.7132C>G | XP_011512317.1:p.Pro2378Ala | |
| XM_005248280.3:c.7132C>G | XP_005248337.1:p.Pro2378Ala | |
| XM_005248282.5:c.6472C>G | XP_005248339.3:p.Pro2158Ala | |
| XM_006714468.2:c.6934C>G | XP_006714531.1:p.Pro2312Ala | |
| XM_017009329.1:c.7132C>G | XP_016864818.1:p.Pro2378Ala | |
| XM_017009330.2:c.5515C>G | XP_016864819.1:p.Pro1839Ala | |
| XM_017009331.1:c.5506C>G | XP_016864820.1:p.Pro1836Ala | |
| NM_133433.4:c.7132C>G MANE Select | NP_597677.2:p.Pro2378Ala | |
| NM_015384.5:c.7132C>G | NP_056199.2:p.Pro2378Ala |