Linked Data
dbSNP Id:
rs3761548
gnomAD v3:
X-49261784-G-T
gnomAD v4:
X-49261784-G-T
MyVariant Identifiers:
chrX:g.49261784G>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.49261784G>T , CM000685.2:g.49261784G>T | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000703450.1:c.-22-3257C>A | ENSP00000515301.1:n.-22-3257C>A | |
| ENST00000684155.1:c.-23+2877C>A | ENSP00000507726.1:n.-23+2877C>A | |
| ENST00000376199.7:c.-23+2877C>A | ENSP00000365372.2:n.-23+2877C>A | |
| ENST00000376207.10:c.-23+2877C>A MANE Select | ENSP00000365380.4:n.-23+2877C>A | |
| ENST00000455775.7:c.-23+2877C>A | ENSP00000396415.3:n.-23+2877C>A | |
| ENST00000557224.6:c.-23+2877C>A | ENSP00000451208.1:n.-23+2877C>A | |
| ENST00000650877.1:c.-22-3257C>A | ENSP00000499100.1:n.-22-3257C>A | |
| ENST00000652559.1:c.-23+2877C>A | ENSP00000498236.1:n.-23+2877C>A | |
| ENST00000376199.6:c.-23+2877C>A | ENSP00000365372.2:n.-23+2877C>A | |
| ENST00000376207.8:c.-23+2877C>A | ENSP00000365380.4:n.-23+2877C>A | |
| ENST00000455775.6:c.-23+2877C>A | ENSP00000396415.3:n.-23+2877C>A | |
| NM_001114377.1:c.-23+2877C>A | NP_001107849.1:n.-23+2877C>A | |
| NM_014009.3:c.-23+2877C>A , LRG_62t1:c.-23+2877C>A | NP_054728.2:n.-23+2877C>A | |
| XM_006724533.2:c.-23+2877C>A | XP_006724596.2:n.-23+2877C>A | |
| XM_011543915.1:c.302+2877C>A | XP_011542217.1:n.302+2877C>A | |
| XM_011543916.1:c.302+2877C>A | XP_011542218.1:n.302+2877C>A | |
| XM_011543917.1:c.-23+2877C>A | XP_011542219.1:n.-23+2877C>A | |
| XM_011543918.1:c.302+2877C>A | XP_011542220.1:n.302+2877C>A | |
| XM_011543919.1:c.302+2877C>A | XP_011542221.1:n.302+2877C>A | |
| XM_017029567.1:c.29+2747C>A | XP_016885056.1:n.29+2747C>A | |
| NM_001114377.2:c.-23+2877C>A | NP_001107849.1:n.-23+2877C>A | |
| NM_014009.4:c.-23+2877C>A MANE Select | NP_054728.2:n.-23+2877C>A |