Linked Data
MyVariant Identifiers:
chr12:g.6127757T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.6018591T>A , CM000674.2:g.6018591T>A | GRCh38 |
| NC_000012.11:g.6127757T>A , CM000674.1:g.6127757T>A | GRCh37 |
| NC_000012.10:g.5998018T>A | NCBI36 |
| NG_009072.1:g.111080A>T | |
| NG_009072.2:g.111080A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000261405.10:c.4827A>T MANE Select | ENSP00000261405.5:p.Gly1609= | |
| ENST00000261405.9:c.4827A>T | ENSP00000261405.5:p.Gly1609= | |
| ENST00000538635.5:n.421-24657A>T | ||
| NM_000552.3:c.4827A>T | NP_000543.2:p.Gly1609= | |
| NM_000552.4:c.4827A>T | NP_000543.2:p.Gly1609= | |
| NM_000552.5:c.4827A>T MANE Select | NP_000543.3:p.Gly1609= |