Linked Data
MyVariant Identifiers:
chr6:g.31784220T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31816443T>C , CM000668.2:g.31816443T>C | GRCh38 |
| NC_000006.11:g.31784220T>C , CM000668.1:g.31784220T>C | GRCh37 |
| NC_000006.10:g.31892199T>C | NCBI36 |
| NG_011855.1:g.3616A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375651.7:c.687T>C (HSPA1A) MANE Select | ENSP00000364802.5:p.Gly229= | |
| ENST00000375651.6:c.687T>C (HSPA1A) | ENSP00000364802.5:p.Gly229= | |
| ENST00000608703.1:c.192T>C (HSPA1A) | ENSP00000477378.1:p.Gly64= | |
| NM_005345.5:c.687T>C (HSPA1A) | NP_005336.3:p.Gly229= | |
| XM_005249073.2:c.-13-4458A>G (HSPA1L) | XP_005249130.1:n.-13-4458A>G | |
| XM_011514566.1:c.-13-4458A>G (HSPA1L) | XP_011512868.1:n.-13-4458A>G | |
| NM_005345.6:c.687T>C (HSPA1A) MANE Select | NP_005336.3:p.Gly229= |