MyVariant.info:
GRCh37
chr4:g.178231152C>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.177309998C>T , CM000666.2:g.177309998C>T | GRCh38 |
| NC_000004.11:g.178231152C>T , CM000666.1:g.178231152C>T | GRCh37 |
| NC_000004.10:g.178468146C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264596.4:c.45C>T MANE Select | ENSP00000264596.3:p.Arg15= | |
| ENST00000264596.3:c.45C>T | ENSP00000264596.3:p.Arg15= | |
| ENST00000513321.1:c.45C>T | ENSP00000424735.1:p.Arg15= | |
| NM_018248.2:c.45C>T | NP_060718.2:p.Arg15= | |
| XM_017008360.1:c.45C>T | XP_016863849.1:p.Arg15= | |
| NM_018248.3:c.45C>T MANE Select | NP_060718.3:p.Arg15= |