Linked Data
MyVariant Identifiers:
chrX:g.119064055G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.119930092G>T , CM000685.2:g.119930092G>T | GRCh38 |
| NC_000023.10:g.119064055G>T , CM000685.1:g.119064055G>T | GRCh37 |
| NC_000023.9:g.118948083G>T | NCBI36 |
| NG_021260.1:g.18681C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000371410.5:c.997C>A MANE Select | ENSP00000360464.3:p.Arg333= | |
| ENST00000652253.1:c.993C>A | ||
| ENST00000371410.4:c.997C>A | ENSP00000360464.3:p.Arg333= | |
| ENST00000477789.5:n.1925C>A | ||
| NM_024528.3:c.997C>A | NP_078804.2:p.Arg333= | |
| XM_017029842.1:c.700C>A | XP_016885331.1:p.Arg234= | |
| NM_024528.4:c.997C>A MANE Select | NP_078804.2:p.Arg333= |