HGVS | Genome Assembly |
---|---|
NC_000002.12:g.219418456C= , CM000664.2:g.219418456C= | GRCh38 |
NC_000002.11:g.220283178C= , CM000664.1:g.220283178C= | GRCh37 |
NC_000002.10:g.219991422C= | NCBI36 |
NG_008043.1:g.5080C= , LRG_380:g.5080C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373960.4:c.-7C= MANE Select | ENSP00000363071.3:n.-7C= | |
ENST00000373960.3:c.-7C= | ENSP00000363071.3:n.-7C= | |
NM_001927.3:c.-7C= , LRG_380t1:c.-7C= | NP_001918.3:n.-7C= | |
NM_001927.4:c.-7C= MANE Select | NP_001918.3:n.-7C= | |
NM_001382708.1:c.-7C= | NP_001369637.1:n.-7C= | |
NM_001382709.1:c.-7C= | NP_001369638.1:n.-7C= | |
NM_001382710.1:c.-7C= | NP_001369639.1:n.-7C= | |
NM_001382711.1:c.-7C= | NP_001369640.1:n.-7C= | |
NM_001382712.1:c.-7C= | NP_001369641.1:n.-7C= | |
NM_001382713.1:c.-7C= | NP_001369642.1:n.-7C= |