Linked Data
ClinVar Variation Id:
2999074
ClinVar RCV Id:
RCV003851705
dbSNP Id:
rs756209419
ExAC:
X:41333853 G / A
gnomAD v2:
X-41333853-G-A
gnomAD v3:
X-41474600-G-A
gnomAD v4:
X-41474600-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.41474600G>A , CM000685.2:g.41474600G>A | GRCh38 |
| NC_000023.10:g.41333853G>A , CM000685.1:g.41333853G>A | GRCh37 |
| NC_000023.9:g.41218797G>A | NCBI36 |
| NG_009112.1:g.32141G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342595.3:c.1132G>A | ENSP00000340328.3:p.Asp378Asn | |
| ENST00000378220.3:c.1132G>A MANE Select | ENSP00000367465.2:p.Asp378Asn | |
| ENST00000378220.2:c.1147G>A | ENSP00000367465.1:p.Asp383Asn | |
| ENST00000342595.2:c.1147G>A | ENSP00000340328.2:p.Asp383Asn | |
| ENST00000378220.1:c.1147G>A | ENSP00000367465.1:p.Asp383Asn | |
| NM_022567.2:c.1147G>A | NP_072089.1:p.Asp383Asn | |
| XM_005272632.2:c.1147G>A | XP_005272689.1:p.Asp383Asn | |
| XM_017029709.1:c.1147G>A | XP_016885198.1:p.Asp383Asn | |
| NM_001378477.3:c.1132G>A MANE Select | NP_001365406.2:p.Asp378Asn | |
| NM_022567.3:c.1132G>A | NP_072089.2:p.Asp378Asn |