HGVS | Genome Assembly |
---|---|
NC_000005.10:g.74685287C= , CM000667.2:g.74685287C= | GRCh38 |
NC_000005.9:g.73981112C= , CM000667.1:g.73981112C= | GRCh37 |
NC_000005.8:g.74016868C= | NCBI36 |
NG_009770.1:g.5144C= | |
NG_009770.2:g.50265C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261416.12:c.27C= MANE Select | ENSP00000261416.7:p.Pro9= | |
ENST00000261416.11:c.27C= | ENSP00000261416.7:p.Pro9= | |
ENST00000511181.5:c.-376-4041C= | ENSP00000426285.1:n.-376-4041C= | |
ENST00000513079.5:n.92C= | ||
ENST00000515528.1:n.82C= | ||
NM_000521.3:c.27C= | NP_000512.1:p.Pro9= | |
NM_001292004.1:c.-376-4041C= | NP_001278933.1:n.-376-4041C= | |
NM_000521.4:c.27C= MANE Select | NP_000512.2:p.Pro9= | |
NM_001292004.2:c.-376-4041C= | NP_001278933.1:n.-376-4041C= |