HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31271492A>G , CM000668.2:g.31271492A>G | GRCh38 |
NC_000006.11:g.31239269A>G , CM000668.1:g.31239269A>G | GRCh37 |
NC_000006.10:g.31347248A>G | NCBI36 |
NG_029422.2:g.5640T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376228.10:c.343+107T>C MANE Select | ENSP00000365402.5:n.343+107T>C | |
ENST00000376228.9:c.343+107T>C | ENSP00000365402.5:n.343+107T>C | |
ENST00000376237.8:c.343+107T>C | ENSP00000365412.4:n.343+107T>C | |
ENST00000383329.7:c.343+107T>C | ENSP00000372819.3:n.343+107T>C | |
ENST00000415537.1:c.341+107T>C | ||
ENST00000484378.1:n.469T>C | ||
ENST00000487245.5:n.559T>C | ||
ENST00000495835.1:n.532+107T>C | ||
NM_002117.5:c.343+107T>C | NP_002108.4:n.343+107T>C | |
NM_002117.6:c.343+107T>C MANE Select | NP_002108.4:n.343+107T>C |