MyVariant.info:
GRCh37
chr19:g.45412277C>A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.44909020C>A , CM000681.2:g.44909020C>A | GRCh38 |
| NC_000019.9:g.45412277C>A , CM000681.1:g.45412277C>A | GRCh37 |
| NC_000019.8:g.50104117C>A | NCBI36 |
| NG_007084.2:g.8239C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252486.9:c.724C>A MANE Select | ENSP00000252486.3:p.Arg242= | |
| ENST00000252486.8:c.724C>A | ENSP00000252486.3:p.Arg242= | |
| ENST00000434152.5:c.802C>A | ENSP00000413653.2:p.Arg268= | |
| NM_000041.3:c.724C>A | NP_000032.1:p.Arg242= | |
| NM_001302688.1:c.802C>A | NP_001289617.1:p.Arg268= | |
| NM_001302689.1:c.724C>A | NP_001289618.1:p.Arg242= | |
| NM_001302690.1:c.724C>A | NP_001289619.1:p.Arg242= | |
| NM_001302691.1:c.724C>A | NP_001289620.1:p.Arg242= | |
| NM_000041.4:c.724C>A MANE Select | NP_000032.1:p.Arg242= | |
| NM_001302688.2:c.802C>A | NP_001289617.1:p.Arg268= | |
| NM_001302689.2:c.724C>A | NP_001289618.1:p.Arg242= | |
| NM_001302691.2:c.724C>A | NP_001289620.1:p.Arg242= | |
| NM_001302690.2:c.724C>A | NP_001289619.1:p.Arg242= |