HGVS | Genome Assembly |
---|---|
NC_000007.14:g.21880688C>T , CM000669.2:g.21880688C>T | GRCh38 |
NC_000007.13:g.21920306C>T , CM000669.1:g.21920306C>T | GRCh37 |
NC_000007.12:g.21886831C>T | NCBI36 |
NG_012886.2:g.342474C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000409508.8:c.12196-14C>T MANE Select | ENSP00000475939.1:n.12196-14C>T | |
ENST00000328843.10:c.12217-14C>T | ENSP00000330671.7:n.12217-14C>T | |
ENST00000409508.7:c.12196-14C>T | ENSP00000475939.1:n.12196-14C>T | |
ENST00000620169.4:c.12217-14C>T | ENSP00000481693.1:n.12217-14C>T | |
NM_001277115.1:c.12196-14C>T | NP_001264044.1:n.12196-14C>T | |
NM_001277115.2:c.12196-14C>T MANE Select | NP_001264044.1:n.12196-14C>T |