MyVariant.info:
GRCh37
chr1:g.197396666C>T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.197427536C>T , CM000663.2:g.197427536C>T | GRCh38 |
| NC_000001.10:g.197396666C>T , CM000663.1:g.197396666C>T | GRCh37 |
| NC_000001.9:g.195663289C>T | NCBI36 |
| NG_008483.1:g.164259C>T | |
| NG_008483.2:g.231075C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367400.8:c.2211C>T MANE Select | ENSP00000356370.3:p.Ile737= | |
| ENST00000638467.1:c.2211C>T | ENSP00000491102.1:p.Ile737= | |
| ENST00000681519.1:c.1092C>T | ENSP00000505267.1:p.Ile364= | |
| ENST00000367397.1:c.354C>T | ENSP00000356367.1:p.Ile118= | |
| ENST00000367399.6:c.1875C>T | ENSP00000356369.2:p.Ile625= | |
| ENST00000367400.7:c.2211C>T | ENSP00000356370.3:p.Ile737= | |
| ENST00000480086.2:n.112C>T | ||
| ENST00000484075.5:c.2211C>T | ENSP00000433932.1:p.Ile737= | |
| ENST00000535699.5:c.2004C>T | ENSP00000438786.1:p.Ile668= | |
| ENST00000538660.5:c.2128+5580C>T | ENSP00000438091.1:n.2128+5580C>T | |
| NM_001193640.1:c.1875C>T | NP_001180569.1:p.Ile625= | |
| NM_001257965.1:c.2004C>T | NP_001244894.1:p.Ile668= | |
| NM_001257966.1:c.2128+5580C>T | NP_001244895.1:n.2128+5580C>T | |
| NM_201253.2:c.2211C>T | NP_957705.1:p.Ile737= | |
| NR_047563.1:n.2212C>T | ||
| NR_047564.1:n.2420C>T | ||
| XM_011509365.1:c.2211C>T | XP_011507667.1:p.Ile737= | |
| XM_011509366.1:c.2211C>T | XP_011507668.1:p.Ile737= | |
| XM_011509367.1:c.2211C>T | XP_011507669.1:p.Ile737= | |
| XM_011509368.1:c.1629C>T | XP_011507670.1:p.Ile543= | |
| XM_011509369.1:c.654C>T | XP_011507671.1:p.Ile218= | |
| XM_011509365.2:c.2211C>T | XP_011507667.1:p.Ile737= | |
| XM_011509369.2:c.654C>T | XP_011507671.1:p.Ile218= | |
| XM_017000851.1:c.1368C>T | XP_016856340.1:p.Ile456= | |
| XM_017000852.1:c.2211C>T | XP_016856341.1:p.Ile737= | |
| NM_201253.3:c.2211C>T MANE Select | NP_957705.1:p.Ile737= | |
| NM_001193640.2:c.1875C>T | NP_001180569.1:p.Ile625= | |
| NM_001257965.2:c.2004C>T | NP_001244894.1:p.Ile668= | |
| NR_047563.2:n.2164C>T | ||
| NR_047564.2:n.2372C>T | ||
| NM_001257966.2:c.2128+5580C>T | NP_001244895.1:n.2128+5580C>T |