HGVS | Genome Assembly |
---|---|
NC_000002.12:g.202377301_202377319del , CM000664.2:g.202377301_202377319del | GRCh38 |
NC_000002.11:g.203242024_203242042del , CM000664.1:g.203242024_203242042del | GRCh37 |
NC_000002.10:g.202950269_202950287del | NCBI36 |
NG_009363.1:g.5975_5993del , LRG_712:g.5975_5993del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374580.10:c.-174_-156del MANE Select | ENSP00000363708.4:n.-174_-156del | |
ENST00000374580.8:c.-174_-156del | ENSP00000363708.4:n.-174_-156del | |
NM_001204.6:c.-174_-156del , LRG_712t1:c.-174_-156del | NP_001195.2:n.-174_-156del | |
XM_011511687.1:c.-174_-156del | XP_011509989.1:n.-174_-156del | |
XM_011511688.1:c.-174_-156del | XP_011509990.1:n.-174_-156del | |
NM_001204.7:c.-174_-156del MANE Select | NP_001195.2:n.-174_-156del |