Linked Data
MyVariant Identifiers:
chr6:g.18130971A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.18130740A>T , CM000668.2:g.18130740A>T | GRCh38 |
| NC_000006.11:g.18130971A>T , CM000668.1:g.18130971A>T | GRCh37 |
| NC_000006.10:g.18238950A>T | NCBI36 |
| NG_012137.2:g.29404T>A | |
| NG_012137.3:g.29404T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309983.5:c.666T>A MANE Select | ENSP00000312304.4:p.Ala222= | |
| ENST00000309983.4:c.666T>A | ENSP00000312304.4:p.Ala222= | |
| NM_000367.3:c.666T>A | NP_000358.1:p.Ala222= | |
| XM_011514839.1:c.621T>A | XP_011513141.1:p.Ala207= | |
| XM_011514840.1:c.597T>A | XP_011513142.1:p.Ala199= | |
| NM_000367.4:c.666T>A | NP_000358.1:p.Ala222= | |
| NM_001346817.1:c.666T>A | NP_001333746.1:p.Ala222= | |
| NM_001346818.1:c.621T>A | NP_001333747.1:p.Ala207= | |
| NM_000367.5:c.666T>A MANE Select | NP_000358.1:p.Ala222= |