Linked Data
dbSNP Id:
rs1328161217
gnomAD v3:
X-154896258-T-G
gnomAD v4:
X-154896258-T-G
MyVariant Identifiers:
chrX:g.154896258T>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154896258T>G , CM000685.2:g.154896258T>G | GRCh38 |
| NC_000023.10:g.154124533T>G , CM000685.1:g.154124533T>G | GRCh37 |
| NC_000023.9:g.153777727T>G | NCBI36 |
| NG_011403.1:g.131466A>C | |
| NG_011403.2:g.131466A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000360256.9:c.6274-26A>C MANE Select | ENSP00000353393.4:n.6274-26A>C | |
| ENST00000360256.8:c.6274-26A>C | ENSP00000353393.4:n.6274-26A>C | |
| NM_000132.3:c.6274-26A>C | NP_000123.1:n.6274-26A>C | |
| XM_011531126.1:c.6169-26A>C | XP_011529428.1:n.6169-26A>C | |
| NM_000132.4:c.6274-26A>C MANE Select | NP_000123.1:n.6274-26A>C |