HGVS | Genome Assembly |
---|---|
NC_000013.11:g.48459415G= , CM000675.2:g.48459415G= | GRCh38 |
NC_000013.10:g.49033551G= , CM000675.1:g.49033551G= | GRCh37 |
NC_000013.9:g.47931552G= | NCBI36 |
NG_009009.1:g.160669G= , LRG_517:g.160669G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000267163.6:c.1961-273G= MANE Select | ENSP00000267163.4:n.1961-273G= | |
ENST00000643064.1:c.194+77972G= | ||
ENST00000650461.1:c.1961-273G= | ENSP00000497193.1:n.1961-273G= | |
ENST00000267163.4:c.1961-273G= | ENSP00000267163.4:n.1961-273G= | |
NM_000321.2:c.1961-273G= , LRG_517t1:c.1961-273G= | NP_000312.2:n.1961-273G= | |
XM_011535171.1:c.1700-273G= | XP_011533473.1:n.1700-273G= | |
XM_011535171.2:c.1700-273G= | XP_011533473.1:n.1700-273G= | |
NM_000321.3:c.1961-273G= MANE Select | NP_000312.2:n.1961-273G= |