Linked Data
dbSNP Id:
rs1398469157
gnomAD v2:
X-25028301-G-C
gnomAD v3:
X-25010184-G-C
gnomAD v4:
X-25010184-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.25010184G>C , CM000685.2:g.25010184G>C | GRCh38 |
| NC_000023.10:g.25028301G>C , CM000685.1:g.25028301G>C | GRCh37 |
| NC_000023.9:g.24938222G>C | NCBI36 |
| NG_008281.1:g.10765C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000379044.5:c.1119+76C>G MANE Select | ENSP00000368332.4:n.1119+76C>G | |
| ENST00000379044.4:c.1119+76C>G | ENSP00000368332.4:n.1119+76C>G | |
| NM_139058.2:c.1119+76C>G | NP_620689.1:n.1119+76C>G | |
| NM_139058.3:c.1119+76C>G MANE Select | NP_620689.1:n.1119+76C>G |