Linked Data
MyVariant Identifiers:
chr1:g.169454888G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169485650G>C , CM000663.2:g.169485650G>C | GRCh38 |
| NC_000001.10:g.169454888G>C , CM000663.1:g.169454888G>C | GRCh37 |
| NC_000001.9:g.167721512G>C | NCBI36 |
| NG_008255.1:g.5321C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000236137.10:c.117C>G MANE Select | ENSP00000236137.5:p.Ala39= | |
| ENST00000646596.1:c.117C>G | ENSP00000494404.1:p.Ala39= | |
| ENST00000236137.9:c.117C>G | ENSP00000236137.5:p.Ala39= | |
| ENST00000367804.4:c.117C>G | ENSP00000356778.3:p.Ala39= | |
| NM_006996.2:c.117C>G | NP_008927.1:p.Ala39= | |
| XM_011509076.1:c.12+403C>G | XP_011507378.1:n.12+403C>G | |
| XM_011509077.1:c.117C>G | XP_011507379.1:p.Ala39= | |
| NM_001319667.1:c.117C>G | NP_001306596.1:p.Ala39= | |
| NM_006996.3:c.117C>G MANE Select | NP_008927.1:p.Ala39= |