HGVS | Genome Assembly |
---|---|
NC_000002.12:g.169348263T= , CM000664.2:g.169348263T= | GRCh38 |
NC_000002.11:g.170204773T= , CM000664.1:g.170204773T= | GRCh37 |
NC_000002.10:g.169913019T= | NCBI36 |
NG_012634.1:g.19350A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000649046.1:c.79+14058A= MANE Select | ENSP00000496870.1:n.79+14058A= | |
ENST00000263816.7:c.79+14058A= | ENSP00000263816.3:n.79+14058A= | |
ENST00000443831.1:c.79+14058A= | ENSP00000409813.1:n.79+14058A= | |
NM_004525.2:c.79+14058A= | NP_004516.2:n.79+14058A= | |
XM_011511183.1:c.79+14058A= | XP_011509485.1:n.79+14058A= | |
XM_011511185.1:c.79+14058A= | XP_011509487.1:n.79+14058A= | |
NM_004525.3:c.79+14058A= MANE Select | NP_004516.2:n.79+14058A= | |
XM_011511183.3:c.79+14058A= | XP_011509485.1:n.79+14058A= |