Linked Data
dbSNP Id:
rs1897692865
gnomAD v3:
15-88881403-A-G
gnomAD v4:
15-88881403-A-G
MyVariant Identifiers:
chr15:g.89424634A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.88881403A>G , CM000677.2:g.88881403A>G | GRCh38 |
| NC_000015.9:g.89424634A>G , CM000677.1:g.89424634A>G | GRCh37 |
| NC_000015.8:g.87225638A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000359595.8:c.447T>C MANE Select | ENSP00000352606.4:p.Ile149= | |
| ENST00000359595.7:c.447T>C | ENSP00000352606.3:p.Ile149= | |
| ENST00000558770.5:c.447T>C | ENSP00000456458.1:p.Ile149= | |
| ENST00000562281.1:c.447T>C | ENSP00000456985.1:p.Ile149= | |
| ENST00000562889.5:c.633T>C | ENSP00000457180.1:p.Ile211= | |
| ENST00000563808.1:n.549T>C | ||
| NM_001307952.1:c.633T>C | NP_001294881.1:p.Ile211= | |
| NM_178232.2:c.447T>C | NP_839946.1:p.Ile149= | |
| NM_178232.3:c.447T>C | NP_839946.1:p.Ile149= | |
| XM_011521261.1:c.579T>C | XP_011519563.1:p.Ile193= | |
| XR_243204.1:n.662T>C | ||
| XR_931756.1:n.768T>C | ||
| XM_017021934.2:c.633T>C | XP_016877423.1:p.Ile211= | |
| XM_017021935.2:c.68T>C | XP_016877424.1:p.Leu23Ser | |
| XM_017021936.2:c.68T>C | XP_016877425.1:p.Leu23Ser | |
| XR_001751098.2:n.780T>C | ||
| XR_931756.3:n.781T>C | ||
| NM_001307952.2:c.633T>C | NP_001294881.1:p.Ile211= | |
| NM_178232.4:c.447T>C MANE Select | NP_839946.1:p.Ile149= |