Linked Data
MyVariant Identifiers:
chrX:g.154091446T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154863171T>G , CM000685.2:g.154863171T>G | GRCh38 |
| NC_000023.10:g.154091446T>G , CM000685.1:g.154091446T>G | GRCh37 |
| NC_000023.9:g.153744640T>G | NCBI36 |
| NG_011403.1:g.164553A>C | |
| NG_011403.2:g.164553A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000360256.9:c.6486A>C MANE Select | ENSP00000353393.4:p.Pro2162= | |
| ENST00000644698.1:c.219A>C | ENSP00000495706.1:p.Pro73= | |
| ENST00000330287.10:c.81A>C | ENSP00000327895.6:p.Pro27= | |
| ENST00000360256.8:c.6486A>C | ENSP00000353393.4:p.Pro2162= | |
| NM_000132.3:c.6486A>C | NP_000123.1:p.Pro2162= | |
| NM_019863.2:c.81A>C | NP_063916.1:p.Pro27= | |
| XM_011531126.1:c.6381A>C | XP_011529428.1:p.Pro2127= | |
| NM_000132.4:c.6486A>C MANE Select | NP_000123.1:p.Pro2162= | |
| NM_019863.3:c.81A>C | NP_063916.1:p.Pro27= |