HGVS | Genome Assembly |
---|---|
NC_000019.10:g.7116859C>T , CM000681.2:g.7116859C>T | GRCh38 |
NC_000019.9:g.7116870C>T , CM000681.1:g.7116870C>T | GRCh37 |
NC_000019.8:g.7067870C>T | NCBI36 |
NG_008852.2:g.182142G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000302850.10:c.*197G>A MANE Select | ENSP00000303830.4:n.*197G>A | |
ENST00000302850.9:c.*197G>A | ENSP00000303830.4:n.*197G>A | |
ENST00000341500.9:c.*197G>A | ENSP00000342838.4:n.*197G>A | |
NM_000208.2:c.*197G>A | NP_000199.2:n.*197G>A | |
NM_000208.3:c.*197G>A | NP_000199.2:n.*197G>A | |
NM_001079817.1:c.*197G>A | NP_001073285.1:n.*197G>A | |
NM_001079817.2:c.*197G>A | NP_001073285.1:n.*197G>A | |
XM_011527988.1:c.*197G>A | XP_011526290.1:n.*197G>A | |
XM_011527989.1:c.*197G>A | XP_011526291.1:n.*197G>A | |
XM_011527988.2:c.*197G>A | XP_011526290.2:n.*197G>A | |
XM_011527989.3:c.*197G>A | XP_011526291.2:n.*197G>A | |
NM_000208.4:c.*197G>A MANE Select | NP_000199.2:n.*197G>A | |
NM_001079817.3:c.*197G>A | NP_001073285.1:n.*197G>A |