Linked Data
dbSNP Id:
rs17759659
gnomAD v2:
18-60958644-A-G
gnomAD v3:
18-63291411-A-G
gnomAD v4:
18-63291411-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.63291411A>G , CM000680.2:g.63291411A>G | GRCh38 |
| NC_000018.9:g.60958644A>G , CM000680.1:g.60958644A>G | GRCh37 |
| NC_000018.8:g.59109624A>G | NCBI36 |
| NG_009361.1:g.32970T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000333681.5:c.585+26671T>C MANE Select | ENSP00000329623.3:n.585+26671T>C | |
| ENST00000677227.1:c.586-10197T>C | ENSP00000504566.1:n.586-10197T>C | |
| ENST00000678134.1:c.789+10251T>C | ENSP00000503628.1:n.789+10251T>C | |
| ENST00000678349.1:c.1137+26119T>C | ENSP00000504190.1:n.1137+26119T>C | |
| ENST00000333681.4:c.585+26671T>C | ENSP00000329623.3:n.585+26671T>C | |
| ENST00000398117.1:c.585+26671T>C | ENSP00000381185.1:n.585+26671T>C | |
| NM_000633.2:c.585+26671T>C | NP_000624.2:n.585+26671T>C | |
| XR_935246.1:n.1698-10197T>C | ||
| XR_935247.1:n.1698-10197T>C | ||
| XR_935248.1:n.1477-10197T>C | ||
| XR_935248.3:n.1979-10197T>C | ||
| NM_000633.3:c.585+26671T>C MANE Select | NP_000624.2:n.585+26671T>C |