HGVS | Genome Assembly |
---|---|
NC_000016.10:g.56982139A= , CM000678.2:g.56982139A= | GRCh38 |
NC_000016.9:g.57016051A= , CM000678.1:g.57016051A= | GRCh37 |
NC_000016.8:g.55573552A= | NCBI36 |
NG_008952.1:g.25217A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000200676.8:c.1249-26A= MANE Select | ENSP00000200676.3:n.1249-26A= | |
ENST00000650358.1:n.1647-26A= | ||
ENST00000200676.7:c.1249-26A= | ENSP00000200676.3:n.1249-26A= | |
ENST00000379780.6:c.1069-26A= | ENSP00000369106.2:n.1069-26A= | |
ENST00000566128.1:c.1054-26A= | ENSP00000456276.1:n.1054-26A= | |
NM_000078.2:c.1249-26A= | NP_000069.2:n.1249-26A= | |
NM_001286085.1:c.1069-26A= | NP_001273014.1:n.1069-26A= | |
NM_000078.3:c.1249-26A= MANE Select | NP_000069.2:n.1249-26A= | |
NM_001286085.2:c.1069-26A= | NP_001273014.1:n.1069-26A= |