HGVS | Genome Assembly |
---|---|
NC_000009.12:g.130872070C= , CM000671.2:g.130872070C= | GRCh38 |
NC_000009.11:g.133747457C= , CM000671.1:g.133747457C= | GRCh37 |
NC_000009.10:g.132737278C= | NCBI36 |
NG_012034.1:g.163190C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372348.9:c.880-59C= | ENSP00000361423.2:n.880-59C= | |
ENST00000318560.6:c.823-59C= MANE Select | ENSP00000323315.5:n.823-59C= | |
ENST00000372348.7:c.880-59C= | ENSP00000361423.2:n.880-59C= | |
ENST00000318560.5:c.823-59C= | ENSP00000323315.5:n.823-59C= | |
ENST00000372348.6:c.880-59C= | ENSP00000361423.2:n.880-59C= | |
NM_005157.5:c.823-59C= | NP_005148.2:n.823-59C= | |
NM_007313.2:c.880-59C= | NP_009297.2:n.880-59C= | |
NM_005157.6:c.823-59C= MANE Select | NP_005148.2:n.823-59C= | |
NM_007313.3:c.880-59C= | NP_009297.2:n.880-59C= |