Linked Data
dbSNP Id:
rs1331224480
gnomAD v2:
7-19156747-C-G
gnomAD v3:
7-19117124-C-G
gnomAD v4:
7-19117124-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.19117124C>G , CM000669.2:g.19117124C>G | GRCh38 |
| NC_000007.13:g.19156747C>G , CM000669.1:g.19156747C>G | GRCh37 |
| NC_000007.12:g.19123272C>G | NCBI36 |
| NG_008114.1:g.5549G>C | |
| NG_008114.2:g.5549G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000242261.6:c.198G>C MANE Select | ENSP00000242261.5:p.Pro66= | |
| ENST00000242261.5:c.198G>C | ENSP00000242261.5:p.Pro66= | |
| NM_000474.3:c.198G>C | NP_000465.1:p.Pro66= | |
| XM_011515496.1:c.198G>C | XP_011513798.1:p.Pro66= | |
| NR_149001.1:n.549G>C | ||
| NM_000474.4:c.198G>C MANE Select | NP_000465.1:p.Pro66= | |
| NR_149001.2:n.513G>C |