Linked Data
MyVariant Identifiers:
chrX:g.105277548C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.106033557C>T , CM000685.2:g.106033557C>T | GRCh38 |
| NC_000023.10:g.105277548C>T , CM000685.1:g.105277548C>T | GRCh37 |
| NC_000023.9:g.105164204C>T | NCBI36 |
| NG_021252.1:g.10171G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372563.2:c.1191G>A MANE Select | ENSP00000361644.1:p.Glu397= | |
| ENST00000327674.8:c.1191G>A | ENSP00000329374.4:p.Glu397= | |
| ENST00000372563.1:c.1191G>A | ENSP00000361644.1:p.Glu397= | |
| NM_000354.5:c.1191G>A | NP_000345.2:p.Glu397= | |
| XM_006724683.1:c.1221G>A | XP_006724746.1:p.Glu407= | |
| XM_005262180.4:c.*136G>A | XP_005262237.1:n.*136G>A | |
| XM_006724683.2:c.1221G>A | XP_006724746.1:p.Glu407= | |
| NM_000354.6:c.1191G>A MANE Select | NP_000345.2:p.Glu397= |