Linked Data
MyVariant Identifiers:
chr6:g.31784211C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31816434C>G , CM000668.2:g.31816434C>G | GRCh38 |
| NC_000006.11:g.31784211C>G , CM000668.1:g.31784211C>G | GRCh37 |
| NC_000006.10:g.31892190C>G | NCBI36 |
| NG_011855.1:g.3625G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375651.7:c.678C>G (HSPA1A) MANE Select | ENSP00000364802.5:p.Thr226= | |
| ENST00000375651.6:c.678C>G (HSPA1A) | ENSP00000364802.5:p.Thr226= | |
| ENST00000608703.1:c.183C>G (HSPA1A) | ENSP00000477378.1:p.Thr61= | |
| NM_005345.5:c.678C>G (HSPA1A) | NP_005336.3:p.Thr226= | |
| XM_005249073.2:c.-13-4449G>C (HSPA1L) | XP_005249130.1:n.-13-4449G>C | |
| XM_011514566.1:c.-13-4449G>C (HSPA1L) | XP_011512868.1:n.-13-4449G>C | |
| NM_005345.6:c.678C>G (HSPA1A) MANE Select | NP_005336.3:p.Thr226= |