Linked Data
MyVariant Identifiers:
chr1:g.215972313C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215798971C>T , CM000663.2:g.215798971C>T | GRCh38 |
| NC_000001.10:g.215972313C>T , CM000663.1:g.215972313C>T | GRCh37 |
| NC_000001.9:g.214038936C>T | NCBI36 |
| NG_009497.1:g.629426G>A | |
| NG_009497.2:g.629478G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000307340.8:c.9894G>A MANE Select | ENSP00000305941.3:p.Gln3298= | |
| ENST00000674083.1:c.9894G>A | ENSP00000501296.1:p.Gln3298= | |
| ENST00000307340.7:c.9894G>A | ENSP00000305941.3:p.Gln3298= | |
| NM_206933.2:c.9894G>A | NP_996816.2:p.Gln3298= | |
| NM_206933.3:c.9894G>A | NP_996816.2:p.Gln3298= | |
| NM_206933.4:c.9894G>A MANE Select | NP_996816.3:p.Gln3298= |