HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31817066G>C , CM000668.2:g.31817066G>C | GRCh38 |
NC_000006.11:g.31784843G>C , CM000668.1:g.31784843G>C | GRCh37 |
NC_000006.10:g.31892822G>C | NCBI36 |
NG_011855.1:g.2993C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375651.7:c.1310G>C (HSPA1A) MANE Select | ENSP00000364802.5:p.Gly437Ala | |
ENST00000375651.6:c.1310G>C (HSPA1A) | ENSP00000364802.5:p.Gly437Ala | |
ENST00000608703.1:c.815G>C (HSPA1A) | ENSP00000477378.1:p.Gly272Ala | |
NM_005345.5:c.1310G>C (HSPA1A) | NP_005336.3:p.Gly437Ala | |
XM_005249073.2:c.-14+3947C>G (HSPA1L) | XP_005249130.1:n.-14+3947C>G | |
XM_011514566.1:c.-14+3947C>G (HSPA1L) | XP_011512868.1:n.-14+3947C>G | |
NM_005345.6:c.1310G>C (HSPA1A) MANE Select | NP_005336.3:p.Gly437Ala |