Linked Data
MyVariant Identifiers:
chr2:g.241808604G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240869187G>A , CM000664.2:g.240869187G>A | GRCh38 |
| NC_000002.11:g.241808604G>A , CM000664.1:g.241808604G>A | GRCh37 |
| NC_000002.10:g.241457277G>A | NCBI36 |
| NG_008005.1:g.5443G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000307503.4:c.183G>A MANE Select | ENSP00000302620.3:p.Lys61= | |
| ENST00000307503.3:c.183G>A | ENSP00000302620.3:p.Lys61= | |
| ENST00000472436.1:n.203G>A | ||
| NM_000030.2:c.183G>A | NP_000021.1:p.Lys61= | |
| XR_924060.1:n.405+1046C>T | ||
| NM_000030.3:c.183G>A MANE Select | NP_000021.1:p.Lys61= |