Linked Data
MyVariant Identifiers:
chr4:g.187120147C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186198993C>T , CM000666.2:g.186198993C>T | GRCh38 |
| NC_000004.11:g.187120147C>T , CM000666.1:g.187120147C>T | GRCh37 |
| NC_000004.10:g.187357141C>T | NCBI36 |
| NG_007965.1:g.12474C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378802.5:c.711C>T MANE Select | ENSP00000368079.4:p.Pro237= | |
| ENST00000378802.4:c.711C>T | ENSP00000368079.4:p.Pro237= | |
| ENST00000507209.5:n.1552C>T | ||
| NM_207352.3:c.711C>T | NP_997235.3:p.Pro237= | |
| XM_005262935.2:c.711C>T | XP_005262992.1:p.Pro237= | |
| XM_006714184.2:c.315C>T | XP_006714247.1:p.Pro105= | |
| XM_005262935.4:c.711C>T | XP_005262992.1:p.Pro237= | |
| XM_017008037.1:c.315C>T | XP_016863526.1:p.Pro105= | |
| NM_207352.4:c.711C>T MANE Select | NP_997235.3:p.Pro237= |