Linked Data
MyVariant Identifiers:
chr19:g.49469110C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.48965853C>A , CM000681.2:g.48965853C>A | GRCh38 |
| NC_000019.9:g.49469110C>A , CM000681.1:g.49469110C>A | GRCh37 |
| NC_000019.8:g.54160922C>A | NCBI36 |
| NG_008152.1:g.5545C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000331825.11:c.186C>A MANE Select | ENSP00000366525.2:p.Gly62= | |
| ENST00000331825.10:c.186C>A | ENSP00000366525.2:p.Gly62= | |
| ENST00000622577.2:c.186C>A | ENSP00000484043.1:p.Gly62= | |
| NM_000146.3:c.186C>A | NP_000137.2:p.Gly62= | |
| XM_024451447.1:c.696C>A | XP_024307215.1:p.Gly232= | |
| NM_000146.4:c.186C>A MANE Select | NP_000137.2:p.Gly62= |