Linked Data
dbSNP Id:
rs774549130
ExAC:
4:79832701 G / A
gnomAD v2:
4-79832701-G-A
gnomAD v3:
4-78911547-G-A
gnomAD v4:
4-78911547-G-A
COSMIC:
COSM6038748
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.78911547G>A , CM000666.2:g.78911547G>A | GRCh38 |
| NC_000004.11:g.79832701G>A , CM000666.1:g.79832701G>A | GRCh37 |
| NC_000004.10:g.80051725G>A | NCBI36 |
| NG_047162.1:g.140170G>A | |
| NG_053104.1:g.32892C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502613.3:c.3000G>A (BMP2K) MANE Select | ENSP00000424668.2:p.Thr1000= | |
| ENST00000335016.9:c.3000G>A (BMP2K) | ENSP00000334836.5:p.Thr1000= | |
| ENST00000342820.10:c.*782+3663C>T (PAQR3) | ENSP00000344203.6:n.*782+3663C>T | |
| ENST00000502613.1:c.2077G>A (BMP2K) | ||
| ENST00000511594.5:c.*642C>T (PAQR3) | ENSP00000425080.1:n.*642C>T | |
| ENST00000512760.5:c.*792+3663C>T (PAQR3) | ENSP00000426875.1:n.*792+3663C>T | |
| ENST00000628286.1:c.*1976G>A (BMP2K) | ENSP00000487317.1:n.*1976G>A | |
| NM_198892.1:c.3000G>A (BMP2K) | NP_942595.1:p.Thr1000= | |
| XM_005263117.1:c.2889G>A (BMP2K) | XP_005263174.1:p.Thr963= | |
| XM_011532101.1:c.2760G>A (BMP2K) | XP_011530403.1:p.Thr920= | |
| XR_938694.1:n.1118-5386C>T (PAQR3) | ||
| XM_017008381.1:c.2760G>A (BMP2K) | XP_016863870.1:p.Thr920= | |
| XM_017008382.1:c.2112G>A (BMP2K) | XP_016863871.1:p.Thr704= | |
| XR_938694.3:n.1098-5386C>T (PAQR3) | ||
| NM_198892.2:c.3000G>A (BMP2K) MANE Select | NP_942595.1:p.Thr1000= |