HGVS | Genome Assembly |
---|---|
NC_000011.10:g.55811576T>C , CM000673.2:g.55811576T>C | GRCh38 |
NC_000011.9:g.55579052T>C , CM000673.1:g.55579052T>C | GRCh37 |
NC_000011.8:g.55335628T>C | NCBI36 |
NG_052620.1:g.5210T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000625203.2:c.110T>C MANE Select | ENSP00000485319.1:p.Val37Ala | |
ENST00000333973.3:c.110T>C | ENSP00000335529.2:p.Val37Ala | |
ENST00000623450.1:c.110T>C | ENSP00000485509.1:p.Val37Ala | |
ENST00000625203.1:c.110T>C | ENSP00000485319.1:p.Val37Ala | |
NM_001004738.1:c.110T>C | NP_001004738.1:p.Val37Ala | |
NM_001004738.2:c.110T>C MANE Select | NP_001004738.1:p.Val37Ala |