Linked Data
dbSNP Id:
rs771860599
gnomAD v3:
2-240869217-G-A
gnomAD v4:
2-240869217-G-A
MyVariant Identifiers:
chr2:g.241808634G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240869217G>A , CM000664.2:g.240869217G>A | GRCh38 |
| NC_000002.11:g.241808634G>A , CM000664.1:g.241808634G>A | GRCh37 |
| NC_000002.10:g.241457307G>A | NCBI36 |
| NG_008005.1:g.5473G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000307503.4:c.213G>A MANE Select | ENSP00000302620.3:p.Arg71= | |
| ENST00000307503.3:c.213G>A | ENSP00000302620.3:p.Arg71= | |
| ENST00000472436.1:n.233G>A | ||
| NM_000030.2:c.213G>A | NP_000021.1:p.Arg71= | |
| XR_924060.1:n.405+1016C>T | ||
| NM_000030.3:c.213G>A MANE Select | NP_000021.1:p.Arg71= |