HGVS | Genome Assembly |
---|---|
NC_000003.12:g.129061481A>C , CM000665.2:g.129061481A>C | GRCh38 |
NC_000003.11:g.128780324A>C , CM000665.1:g.128780324A>C | GRCh37 |
NC_000003.10:g.130263014A>C | NCBI36 |
NG_008715.1:g.5680A>C , LRG_477:g.5680A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307395.5:c.-138-13A>C MANE Select | ENSP00000303942.4:n.-138-13A>C | |
ENST00000307395.4:c.-138-13A>C | ENSP00000303942.4:n.-138-13A>C | |
NM_000174.4:c.-138-13A>C , LRG_477t1:c.-138-13A>C | NP_000165.1:n.-138-13A>C | |
XM_005247374.3:c.-138-13A>C | XP_005247431.1:n.-138-13A>C | |
XM_011512701.1:c.-138-13A>C | XP_011511003.1:n.-138-13A>C | |
XM_011512702.1:c.-12-247A>C | XP_011511004.1:n.-12-247A>C | |
NM_000174.5:c.-138-13A>C MANE Select | NP_000165.1:n.-138-13A>C |