Linked Data
ClinVar Variation Id:
2876683
ClinVar RCV Id:
RCV003710442
dbSNP Id:
rs759560622
gnomAD v3:
19-39507400-C-G
gnomAD v4:
19-39507400-C-G
MyVariant Identifiers:
chr19:g.39998040C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.39507400C>G , CM000681.2:g.39507400C>G | GRCh38 |
| NC_000019.9:g.39998040C>G , CM000681.1:g.39998040C>G | GRCh37 |
| NC_000019.8:g.44689880C>G | NCBI36 |
| NG_008256.1:g.13484C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356433.10:c.1455C>G MANE Select | ENSP00000348810.4:p.Pro485= | |
| ENST00000205143.4:c.1455C>G | ENSP00000205143.3:p.Pro485= | |
| ENST00000356433.9:c.1455C>G | ENSP00000348810.4:p.Pro485= | |
| NM_016941.3:c.1455C>G | NP_058637.1:p.Pro485= | |
| NM_203486.2:c.1455C>G | NP_982353.1:p.Pro485= | |
| NM_016941.4:c.1455C>G | NP_058637.1:p.Pro485= | |
| NM_203486.3:c.1455C>G MANE Select | NP_982353.1:p.Pro485= |