Linked Data
MyVariant Identifiers:
chr2:g.96958722A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.96292984A>T , CM000664.2:g.96292984A>T | GRCh38 |
| NC_000002.11:g.96958722A>T , CM000664.1:g.96958722A>T | GRCh37 |
| NC_000002.10:g.96322449A>T | NCBI36 |
| NG_016973.1:g.17576T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000323853.10:c.2148T>A MANE Select | ENSP00000317123.5:p.Ala716= | |
| ENST00000652267.1:c.2148T>A | ENSP00000498933.1:p.Ala716= | |
| ENST00000323853.9:c.2148T>A | ENSP00000317123.5:p.Ala716= | |
| NM_014014.4:c.2148T>A | NP_054733.2:p.Ala716= | |
| NM_014014.5:c.2148T>A MANE Select | NP_054733.2:p.Ala716= |