Linked Data
dbSNP Id:
rs755162991
ExAC:
10:72643680 G / C
gnomAD v2:
10-72643680-G-C
gnomAD v4:
10-70883923-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.70883923G>C , CM000672.2:g.70883923G>C | GRCh38 |
| NC_000010.10:g.72643680G>C , CM000672.1:g.72643680G>C | GRCh37 |
| NC_000010.9:g.72313686G>C | NCBI36 |
| NG_008646.1:g.9862C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000697988.1:c.571-9836G>C (SGPL1) | ENSP00000513492.1:n.571-9836G>C | |
| ENST00000299299.4:c.*27C>G (PCBD1) MANE Select | ENSP00000299299.3:n.*27C>G | |
| ENST00000299299.3:c.*27C>G (PCBD1) | ENSP00000299299.3:n.*27C>G | |
| ENST00000493961.5:n.183+1229C>G (PCBD1) | ||
| NM_000281.3:c.*27C>G (PCBD1) | NP_000272.1:n.*27C>G | |
| NM_001289797.1:c.*27C>G (PCBD1) | NP_001276726.1:n.*27C>G | |
| XM_005269877.1:c.216+1229C>G (PCBD1) | XP_005269934.1:n.216+1229C>G | |
| NM_001323004.1:c.216+1229C>G (PCBD1) | NP_001309933.1:n.216+1229C>G | |
| NM_000281.4:c.*27C>G (PCBD1) MANE Select | NP_000272.1:n.*27C>G | |
| NM_001289797.2:c.*27C>G (PCBD1) | NP_001276726.1:n.*27C>G | |
| NM_001323004.2:c.216+1229C>G (PCBD1) | NP_001309933.1:n.216+1229C>G |