MyVariant.info:
GRCh37
chr9:g.37426542C>A
gnomAD v3:
gnomAD v4:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.37426545C>A , CM000671.2:g.37426545C>A | GRCh38 |
| NC_000009.11:g.37426542C>A , CM000671.1:g.37426542C>A | GRCh37 |
| NC_000009.10:g.37416542C>A | NCBI36 |
| NG_008135.1:g.8836C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000318158.11:c.295C>A MANE Select | ENSP00000313432.6:p.Arg99= | |
| ENST00000318158.10:c.295C>A | ENSP00000313432.6:p.Arg99= | |
| ENST00000377824.8:n.332C>A | ||
| ENST00000460882.5:n.322C>A | ||
| ENST00000487399.5:n.847C>A | ||
| ENST00000491488.5:n.110-1939C>A | ||
| ENST00000493368.5:n.352C>A | ||
| ENST00000607784.1:c.295C>A | ENSP00000475569.1:p.Arg99= | |
| NM_012203.1:c.295C>A | NP_036335.1:p.Arg99= | |
| XM_005251631.1:c.84-1939C>A | XP_005251688.1:n.84-1939C>A | |
| XM_011518073.1:c.-468C>A | XP_011516375.1:n.-468C>A | |
| XR_929374.1:n.380C>A | ||
| XM_017015320.2:c.295C>A | XP_016870809.1:p.Arg99= | |
| XM_017015321.2:c.295C>A | XP_016870810.1:p.Arg99= | |
| XM_017015323.2:c.-468C>A | XP_016870812.1:n.-468C>A | |
| XM_024447716.1:c.568C>A | XP_024303484.1:p.Arg190= | |
| XM_024447717.1:c.568C>A | XP_024303485.1:p.Arg190= | |
| XR_002956828.1:n.583C>A | ||
| XR_002956829.1:n.583C>A | ||
| XR_002956830.1:n.354C>A | ||
| XR_002956831.1:n.139-1939C>A | ||
| XR_002956832.1:n.354C>A | ||
| NM_012203.2:c.295C>A MANE Select | NP_036335.1:p.Arg99= |