Linked Data
dbSNP Id:
rs184218514
gnomAD v3:
18-63279809-A-G
gnomAD v4:
18-63279809-A-G
MyVariant Identifiers:
chr18:g.63279809A>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.63279809A>G , CM000680.2:g.63279809A>G | GRCh38 |
| NC_000018.9:g.60947042A>G , CM000680.1:g.60947042A>G | GRCh37 |
| NC_000018.8:g.59098022A>G | NCBI36 |
| NG_009361.1:g.44572T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000333681.5:c.585+38273T>C MANE Select | ENSP00000329623.3:n.585+38273T>C | |
| ENST00000677227.1:c.913+1078T>C | ENSP00000504566.1:n.913+1078T>C | |
| ENST00000678134.1:c.789+21853T>C | ENSP00000503628.1:n.789+21853T>C | |
| ENST00000678349.1:c.1137+37721T>C | ENSP00000504190.1:n.1137+37721T>C | |
| ENST00000333681.4:c.585+38273T>C | ENSP00000329623.3:n.585+38273T>C | |
| ENST00000398117.1:c.585+38273T>C | ENSP00000381185.1:n.585+38273T>C | |
| NM_000633.2:c.585+38273T>C | NP_000624.2:n.585+38273T>C | |
| XR_935246.1:n.2025+1078T>C | ||
| XR_935247.1:n.2025+1078T>C | ||
| XR_935248.1:n.1804+1078T>C | ||
| XR_935248.3:n.2306+1078T>C | ||
| NM_000633.3:c.585+38273T>C MANE Select | NP_000624.2:n.585+38273T>C |