Linked Data
ClinVar Variation Id:
1121200
ClinVar RCV Id:
RCV001451398
dbSNP Id:
rs1348201363
MyVariant Identifiers:
chr1:g.215953270G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215779928G>T , CM000663.2:g.215779928G>T | GRCh38 |
| NC_000001.10:g.215953270G>T , CM000663.1:g.215953270G>T | GRCh37 |
| NC_000001.9:g.214019893G>T | NCBI36 |
| NG_009497.1:g.648469C>A | |
| NG_009497.2:g.648521C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.10854C>A MANE Select | ENSP00000305941.3:p.Gly3618= | |
| ENST00000674083.1:c.10854C>A | ENSP00000501296.1:p.Gly3618= | |
| ENST00000307340.7:c.10854C>A | ENSP00000305941.3:p.Gly3618= | |
| NM_206933.2:c.10854C>A | NP_996816.2:p.Gly3618= | |
| NM_206933.3:c.10854C>A | NP_996816.2:p.Gly3618= | |
| NM_206933.4:c.10854C>A MANE Select | NP_996816.3:p.Gly3618= |