HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31816432A>G , CM000668.2:g.31816432A>G | GRCh38 |
NC_000006.11:g.31784209A>G , CM000668.1:g.31784209A>G | GRCh37 |
NC_000006.10:g.31892188A>G | NCBI36 |
NG_011855.1:g.3627T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375651.7:c.676A>G (HSPA1A) MANE Select | ENSP00000364802.5:p.Thr226Ala | |
ENST00000375651.6:c.676A>G (HSPA1A) | ENSP00000364802.5:p.Thr226Ala | |
ENST00000608703.1:c.181A>G (HSPA1A) | ENSP00000477378.1:p.Thr61Ala | |
NM_005345.5:c.676A>G (HSPA1A) | NP_005336.3:p.Thr226Ala | |
XM_005249073.2:c.-13-4447T>C (HSPA1L) | XP_005249130.1:n.-13-4447T>C | |
XM_011514566.1:c.-13-4447T>C (HSPA1L) | XP_011512868.1:n.-13-4447T>C | |
NM_005345.6:c.676A>G (HSPA1A) MANE Select | NP_005336.3:p.Thr226Ala |