HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31817230G>T , CM000668.2:g.31817230G>T | GRCh38 |
NC_000006.11:g.31785007G>T , CM000668.1:g.31785007G>T | GRCh37 |
NC_000006.10:g.31892986G>T | NCBI36 |
NG_011855.1:g.2829C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375651.7:c.1474G>T (HSPA1A) MANE Select | ENSP00000364802.5:p.Asp492Tyr | |
ENST00000375651.6:c.1474G>T (HSPA1A) | ENSP00000364802.5:p.Asp492Tyr | |
ENST00000608703.1:c.979G>T (HSPA1A) | ENSP00000477378.1:p.Asp327Tyr | |
NM_005345.5:c.1474G>T (HSPA1A) | NP_005336.3:p.Asp492Tyr | |
XM_005249073.2:c.-14+3783C>A (HSPA1L) | XP_005249130.1:n.-14+3783C>A | |
XM_011514566.1:c.-14+3783C>A (HSPA1L) | XP_011512868.1:n.-14+3783C>A | |
NM_005345.6:c.1474G>T (HSPA1A) MANE Select | NP_005336.3:p.Asp492Tyr |