HGVS | Genome Assembly |
---|---|
NC_000005.10:g.150859919A>T , CM000667.2:g.150859919A>T | GRCh38 |
NC_000005.9:g.150239481A>T , CM000667.1:g.150239481A>T | GRCh37 |
NC_000005.8:g.150219674A>T | NCBI36 |
NG_027809.2:g.18397A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000520549.1:c.158+11265A>T | ||
XM_011537641.1:c.531+11265A>T | XP_011535943.1:n.531+11265A>T | |
NM_001346557.1:c.531+11265A>T | NP_001333486.1:n.531+11265A>T | |
NM_001346557.2:c.531+11265A>T | NP_001333486.1:n.531+11265A>T | |
NR_170598.1:n.1646+11265A>T |