Linked Data
MyVariant Identifiers:
chr4:g.187115730G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186194576G>C , CM000666.2:g.186194576G>C | GRCh38 |
| NC_000004.11:g.187115730G>C , CM000666.1:g.187115730G>C | GRCh37 |
| NC_000004.10:g.187352724G>C | NCBI36 |
| NG_007965.1:g.8057G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000378802.5:c.291G>C MANE Select | ENSP00000368079.4:p.Val97= | |
| ENST00000378802.4:c.291G>C | ENSP00000368079.4:p.Val97= | |
| NM_207352.3:c.291G>C | NP_997235.3:p.Val97= | |
| XM_005262935.2:c.291G>C | XP_005262992.1:p.Val97= | |
| XM_006714184.2:c.-20G>C | XP_006714247.1:n.-20G>C | |
| XM_005262935.4:c.291G>C | XP_005262992.1:p.Val97= | |
| XM_017008037.1:c.-20G>C | XP_016863526.1:n.-20G>C | |
| NM_207352.4:c.291G>C MANE Select | NP_997235.3:p.Val97= |