HGVS | Genome Assembly |
---|---|
NC_000012.12:g.57766159G>A , CM000674.2:g.57766159G>A | GRCh38 |
NC_000012.11:g.58159942G>A , CM000674.1:g.58159942G>A | GRCh37 |
NC_000012.10:g.56446209G>A | NCBI36 |
NG_007076.1:g.6035C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000546609.2:n.146C>T | ||
ENST00000713544.1:c.234C>T | ENSP00000518840.1:p.Ala78= | |
ENST00000713545.1:c.234C>T | ENSP00000518841.1:p.Ala78= | |
ENST00000228606.9:c.234C>T MANE Select | ENSP00000228606.4:p.Ala78= | |
ENST00000228606.8:c.234C>T | ENSP00000228606.4:p.Ala78= | |
ENST00000546496.1:n.62C>T | ||
ENST00000546609.1:c.146C>T | ||
ENST00000547344.5:n.288C>T | ||
ENST00000552186.1:n.353C>T | ||
NM_000785.3:c.234C>T | NP_000776.1:p.Ala78= | |
NM_000785.4:c.234C>T MANE Select | NP_000776.1:p.Ala78= |