HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31816412T>C , CM000668.2:g.31816412T>C | GRCh38 |
NC_000006.11:g.31784189T>C , CM000668.1:g.31784189T>C | GRCh37 |
NC_000006.10:g.31892168T>C | NCBI36 |
NG_011855.1:g.3647A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375651.7:c.656T>C (HSPA1A) MANE Select | ENSP00000364802.5:p.Val219Ala | |
ENST00000375651.6:c.656T>C (HSPA1A) | ENSP00000364802.5:p.Val219Ala | |
ENST00000608703.1:c.161T>C (HSPA1A) | ENSP00000477378.1:p.Val54Ala | |
NM_005345.5:c.656T>C (HSPA1A) | NP_005336.3:p.Val219Ala | |
XM_005249073.2:c.-13-4427A>G (HSPA1L) | XP_005249130.1:n.-13-4427A>G | |
XM_011514566.1:c.-13-4427A>G (HSPA1L) | XP_011512868.1:n.-13-4427A>G | |
NM_005345.6:c.656T>C (HSPA1A) MANE Select | NP_005336.3:p.Val219Ala |