Linked Data
dbSNP Id:
rs370861712
ExAC:
4:79832589 C / T
gnomAD v2:
4-79832589-C-T
gnomAD v3:
4-78911435-C-T
gnomAD v4:
4-78911435-C-T
COSMIC:
COSM196972
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.78911435C>T , CM000666.2:g.78911435C>T | GRCh38 |
| NC_000004.11:g.79832589C>T , CM000666.1:g.79832589C>T | GRCh37 |
| NC_000004.10:g.80051613C>T | NCBI36 |
| NG_047162.1:g.140058C>T | |
| NG_053104.1:g.33004G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502613.3:c.2888C>T (BMP2K) MANE Select | ENSP00000424668.2:p.Thr963Met | |
| ENST00000335016.9:c.2888C>T (BMP2K) | ENSP00000334836.5:p.Thr963Met | |
| ENST00000342820.10:c.*782+3775G>A (PAQR3) | ENSP00000344203.6:n.*782+3775G>A | |
| ENST00000502613.1:c.1965C>T (BMP2K) | ||
| ENST00000511594.5:c.*754G>A (PAQR3) | ENSP00000425080.1:n.*754G>A | |
| ENST00000512760.5:c.*792+3775G>A (PAQR3) | ENSP00000426875.1:n.*792+3775G>A | |
| ENST00000628286.1:c.*1864C>T (BMP2K) | ENSP00000487317.1:n.*1864C>T | |
| NM_198892.1:c.2888C>T (BMP2K) | NP_942595.1:p.Thr963Met | |
| XM_005263117.1:c.2777C>T (BMP2K) | XP_005263174.1:p.Thr926Met | |
| XM_011532101.1:c.2648C>T (BMP2K) | XP_011530403.1:p.Thr883Met | |
| XR_938694.1:n.1118-5274G>A (PAQR3) | ||
| XM_017008381.1:c.2648C>T (BMP2K) | XP_016863870.1:p.Thr883Met | |
| XM_017008382.1:c.2000C>T (BMP2K) | XP_016863871.1:p.Thr667Met | |
| XR_938694.3:n.1098-5274G>A (PAQR3) | ||
| NM_198892.2:c.2888C>T (BMP2K) MANE Select | NP_942595.1:p.Thr963Met |