HGVS | Genome Assembly |
---|---|
NC_000021.9:g.33026379T>C , CM000683.2:g.33026379T>C | GRCh38 |
NC_000021.8:g.34398687T>C , CM000683.1:g.34398687T>C | GRCh37 |
NC_000021.7:g.33320557T>C | NCBI36 |
NG_011834.1:g.5449T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000382357.4:c.-63+353T>C MANE Select | ENSP00000371794.3:n.-63+353T>C | |
ENST00000333337.3:c.-484T>C | ENSP00000331040.3:n.-484T>C | |
ENST00000382357.3:c.-63+353T>C | ENSP00000371794.3:n.-63+353T>C | |
ENST00000430860.1:c.-63+119T>C | ENSP00000391183.1:n.-63+119T>C | |
NM_005806.3:c.-63+353T>C | NP_005797.1:n.-63+353T>C | |
XM_005260908.1:c.-63+119T>C | XP_005260965.1:n.-63+119T>C | |
NM_005806.4:c.-63+353T>C MANE Select | NP_005797.1:n.-63+353T>C |