HGVS | Genome Assembly |
---|---|
NC_000009.12:g.101586165C>G , CM000671.2:g.101586165C>G | GRCh38 |
NC_000009.11:g.104348447C>G , CM000671.1:g.104348447C>G | GRCh37 |
NC_000009.10:g.103388268C>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361820.6:c.2767-6805G>C MANE Select | ENSP00000355155.3:n.2767-6805G>C | |
ENST00000361820.3:c.2767-6805G>C | ENSP00000355155.3:n.2767-6805G>C | |
NM_133445.2:c.2767-6805G>C | NP_597702.2:n.2767-6805G>C | |
NM_133445.3:c.2767-6805G>C MANE Select | NP_597702.2:n.2767-6805G>C |