Linked Data
MyVariant Identifiers:
chrX:g.154132337G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154904062G>A , CM000685.2:g.154904062G>A | GRCh38 |
| NC_000023.10:g.154132337G>A , CM000685.1:g.154132337G>A | GRCh37 |
| NC_000023.9:g.153785531G>A | NCBI36 |
| NG_011403.1:g.123662C>T | |
| NG_011403.2:g.123662C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.5842C>T MANE Select | ENSP00000353393.4:p.Leu1948= | |
| ENST00000360256.8:c.5842C>T | ENSP00000353393.4:p.Leu1948= | |
| NM_000132.3:c.5842C>T | NP_000123.1:p.Leu1948= | |
| XM_011531126.1:c.5737C>T | XP_011529428.1:p.Leu1913= | |
| NM_000132.4:c.5842C>T MANE Select | NP_000123.1:p.Leu1948= |