Linked Data
ClinVar Variation Id:
2747896
ClinVar RCV Id:
RCV003570684
dbSNP Id:
rs2079650462
gnomAD v4:
19-39507454-G-A
MyVariant Identifiers:
chr19:g.39998094G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.39507454G>A , CM000681.2:g.39507454G>A | GRCh38 |
| NC_000019.9:g.39998094G>A , CM000681.1:g.39998094G>A | GRCh37 |
| NC_000019.8:g.44689934G>A | NCBI36 |
| NG_008256.1:g.13538G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356433.10:c.1509G>A MANE Select | ENSP00000348810.4:p.Ala503= | |
| ENST00000205143.4:c.1509G>A | ENSP00000205143.3:p.Ala503= | |
| ENST00000356433.9:c.1509G>A | ENSP00000348810.4:p.Ala503= | |
| NM_016941.3:c.1509G>A | NP_058637.1:p.Ala503= | |
| NM_203486.2:c.1509G>A | NP_982353.1:p.Ala503= | |
| NM_016941.4:c.1509G>A | NP_058637.1:p.Ala503= | |
| NM_203486.3:c.1509G>A MANE Select | NP_982353.1:p.Ala503= |