HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31816422G>T , CM000668.2:g.31816422G>T | GRCh38 |
NC_000006.11:g.31784199G>T , CM000668.1:g.31784199G>T | GRCh37 |
NC_000006.10:g.31892178G>T | NCBI36 |
NG_011855.1:g.3637C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375651.7:c.666G>T (HSPA1A) MANE Select | ENSP00000364802.5:p.Thr222= | |
ENST00000375651.6:c.666G>T (HSPA1A) | ENSP00000364802.5:p.Thr222= | |
ENST00000608703.1:c.171G>T (HSPA1A) | ENSP00000477378.1:p.Thr57= | |
NM_005345.5:c.666G>T (HSPA1A) | NP_005336.3:p.Thr222= | |
XM_005249073.2:c.-13-4437C>A (HSPA1L) | XP_005249130.1:n.-13-4437C>A | |
XM_011514566.1:c.-13-4437C>A (HSPA1L) | XP_011512868.1:n.-13-4437C>A | |
NM_005345.6:c.666G>T (HSPA1A) MANE Select | NP_005336.3:p.Thr222= |