Linked Data
dbSNP Id:
rs1553922653
ExAC:
4:79832610 T / C
gnomAD v2:
4-79832610-T-C
gnomAD v3:
4-78911456-T-C
gnomAD v4:
4-78911456-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.78911456T>C , CM000666.2:g.78911456T>C | GRCh38 |
| NC_000004.11:g.79832610T>C , CM000666.1:g.79832610T>C | GRCh37 |
| NC_000004.10:g.80051634T>C | NCBI36 |
| NG_047162.1:g.140079T>C | |
| NG_053104.1:g.32983A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502613.3:c.2909T>C (BMP2K) MANE Select | ENSP00000424668.2:p.Val970Ala | |
| ENST00000335016.9:c.2909T>C (BMP2K) | ENSP00000334836.5:p.Val970Ala | |
| ENST00000342820.10:c.*782+3754A>G (PAQR3) | ENSP00000344203.6:n.*782+3754A>G | |
| ENST00000502613.1:c.1986T>C (BMP2K) | ||
| ENST00000511594.5:c.*733A>G (PAQR3) | ENSP00000425080.1:n.*733A>G | |
| ENST00000512760.5:c.*792+3754A>G (PAQR3) | ENSP00000426875.1:n.*792+3754A>G | |
| ENST00000628286.1:c.*1885T>C (BMP2K) | ENSP00000487317.1:n.*1885T>C | |
| NM_198892.1:c.2909T>C (BMP2K) | NP_942595.1:p.Val970Ala | |
| XM_005263117.1:c.2798T>C (BMP2K) | XP_005263174.1:p.Val933Ala | |
| XM_011532101.1:c.2669T>C (BMP2K) | XP_011530403.1:p.Val890Ala | |
| XR_938694.1:n.1118-5295A>G (PAQR3) | ||
| XM_017008381.1:c.2669T>C (BMP2K) | XP_016863870.1:p.Val890Ala | |
| XM_017008382.1:c.2021T>C (BMP2K) | XP_016863871.1:p.Val674Ala | |
| XR_938694.3:n.1098-5295A>G (PAQR3) | ||
| NM_198892.2:c.2909T>C (BMP2K) MANE Select | NP_942595.1:p.Val970Ala |