Linked Data
gnomAD v4:
X-151181385-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.151181385A>C , CM000685.2:g.151181385A>C | GRCh38 |
| NC_000023.10:g.150349857A>C , CM000685.1:g.150349857A>C | GRCh37 |
| NC_000023.9:g.150100515A>C | NCBI36 |
| NG_016405.1:g.9802A>C | |
| NG_016405.2:g.9802A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218316.4:c.1802A>C MANE Select | ENSP00000218316.3:p.His601Pro | |
| ENST00000218316.3:c.1802A>C | ENSP00000218316.3:p.His601Pro | |
| ENST00000617907.1:c.1796A>C | ENSP00000484496.1:p.His599Pro | |
| NM_004224.3:c.1802A>C MANE Select | NP_004215.2:p.His601Pro | |
| XM_011531216.1:c.1061A>C | XP_011529518.1:p.His354Pro | |
| XM_011531216.2:c.1061A>C | XP_011529518.1:p.His354Pro |