Linked Data
gnomAD v3:
X-106034283-A-G
gnomAD v4:
X-106034283-A-G
MyVariant Identifiers:
chrX:g.105278274A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.106034283A>G , CM000685.2:g.106034283A>G | GRCh38 |
| NC_000023.10:g.105278274A>G , CM000685.1:g.105278274A>G | GRCh37 |
| NC_000023.9:g.105164930A>G | NCBI36 |
| NG_021252.1:g.9445T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000372563.2:c.996T>C MANE Select | ENSP00000361644.1:p.Asn332= | |
| ENST00000327674.8:c.996T>C | ENSP00000329374.4:p.Asn332= | |
| ENST00000372563.1:c.996T>C | ENSP00000361644.1:p.Asn332= | |
| ENST00000487487.1:n.269T>C | ||
| NM_000354.5:c.996T>C | NP_000345.2:p.Asn332= | |
| XM_005262180.3:c.996T>C | XP_005262237.1:p.Asn332= | |
| XM_006724683.1:c.996T>C | XP_006724746.1:p.Asn332= | |
| XM_005262180.4:c.996T>C | XP_005262237.1:p.Asn332= | |
| XM_006724683.2:c.996T>C | XP_006724746.1:p.Asn332= | |
| NM_000354.6:c.996T>C MANE Select | NP_000345.2:p.Asn332= |