HGVS | Genome Assembly |
---|---|
NC_000012.12:g.68156438G>T , CM000674.2:g.68156438G>T | GRCh38 |
NC_000012.11:g.68550218G>T , CM000674.1:g.68550218G>T | GRCh37 |
NC_000012.10:g.66836485G>T | NCBI36 |
NG_015840.1:g.8304C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000229135.4:c.367-951C>A MANE Select | ENSP00000229135.3:n.367-951C>A | |
ENST00000229135.3:c.367-951C>A | ENSP00000229135.3:n.367-951C>A | |
NM_000619.2:c.367-951C>A | NP_000610.2:n.367-951C>A | |
NM_000619.3:c.367-951C>A MANE Select | NP_000610.2:n.367-951C>A |