HGVS | Genome Assembly |
---|---|
NC_000012.12:g.66209624C= , CM000674.2:g.66209624C= | GRCh38 |
NC_000012.11:g.66603404C= , CM000674.1:g.66603404C= | GRCh37 |
NC_000012.10:g.64889671C= | NCBI36 |
NG_021194.1:g.25427C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261233.9:c.381+104C= MANE Select | ENSP00000261233.4:n.381+104C= | |
ENST00000261233.8:c.381+104C= | ENSP00000261233.4:n.381+104C= | |
ENST00000457197.2:c.198+104C= | ENSP00000409852.2:n.198+104C= | |
NM_001142523.1:c.198+104C= | NP_001135995.1:n.198+104C= | |
NM_007199.2:c.381+104C= | NP_009130.2:n.381+104C= | |
NM_001142523.2:c.198+104C= | NP_001135995.1:n.198+104C= | |
NM_007199.3:c.381+104C= MANE Select | NP_009130.2:n.381+104C= |