HGVS | Genome Assembly |
---|---|
NC_000019.10:g.35848125G= , CM000681.2:g.35848125G= | GRCh38 |
NC_000019.9:g.36339027G= , CM000681.1:g.36339027G= | GRCh37 |
NC_000019.8:g.41030867G= | NCBI36 |
NG_013356.2:g.26163C= , LRG_693:g.26163C= | |
NG_051206.1:g.1491G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000378910.10:c.1356C= MANE Select | ENSP00000368190.4:p.Gly452= | |
ENST00000353632.6:c.1356C= | ENSP00000343634.5:p.Gly452= | |
ENST00000378910.9:c.1356C= | ENSP00000368190.4:p.Gly452= | |
ENST00000592132.1:n.363C= | ||
NM_004646.3:c.1356C= , LRG_693t1:c.1356C= | NP_004637.1:p.Gly452= | |
NM_004646.4:c.1356C= MANE Select | NP_004637.1:p.Gly452= |